Dynamic programming is used for sequence alignment and other bioinformatics tasks. It works by breaking problems down into smaller subproblems. Needleman-Wunsch introduced an algorithm for global sequence alignment using dynamic programming that maximizes matches between sequences. The algorithm involves initializing a matrix, filling it using scoring schemes, and backtracking to trace alignments. Local alignment follows a similar approach but replaces negative values in the matrix with zeros to restrict alignments.
Genome annotation, NGS sequence data, decoding sequence information, The genome contains all the biological information required to build and maintain any given living organism.
Sequence alig Sequence Alignment Pairwise alignment:-naveed ul mushtaq
Sequence Alignment Pairwise alignment:- Global Alignment and Local AlignmentTwo types of alignment Progressive Programs for multiple sequence alignment BLOSUM Point accepted mutation (PAM)PAM VS BLOSUM
In shotgun sequencing the genome is broken randomly into short fragments (1 to 2 kbp long) suitable for sequencing. The fragments are ligated into a suitable vector and then partially sequenced. Around 400–500 bp of sequence can be generated from each fragment in a single sequencing run. In some cases, both ends of a fragment are sequenced. Computerized searching for overlaps between individual sequences then assembles the complete sequence.
Genome annotation, NGS sequence data, decoding sequence information, The genome contains all the biological information required to build and maintain any given living organism.
Sequence alig Sequence Alignment Pairwise alignment:-naveed ul mushtaq
Sequence Alignment Pairwise alignment:- Global Alignment and Local AlignmentTwo types of alignment Progressive Programs for multiple sequence alignment BLOSUM Point accepted mutation (PAM)PAM VS BLOSUM
In shotgun sequencing the genome is broken randomly into short fragments (1 to 2 kbp long) suitable for sequencing. The fragments are ligated into a suitable vector and then partially sequenced. Around 400–500 bp of sequence can be generated from each fragment in a single sequencing run. In some cases, both ends of a fragment are sequenced. Computerized searching for overlaps between individual sequences then assembles the complete sequence.
STS stands for sequence tagged site which is short DNA sequence, generally between 100 and 500 bp in length, that is easily recognizable and occurs only once in the chromosome or genome being studied.
Scoring system is a set of values for qualifying the set of one residue being substituted by another in an alignment.
It is also known as substitution matrix.
Scoring matrix of nucleotide is relatively simple.
A positive value or a high score is given for a match & negative value or a low score is given for a mismatch.
Scoring matrices for amino acids are more complicated because scoring has to reflect the physicochemical properties of amino acid residues.
Ab Initio Protein Structure Prediction is a method to determine the tertiary structure of protein in the absence of experimentally solved structure of a similar/homologous protein. This method builds protein structure guided by energy function.
I had prepared this presentation for an internal project during my masters degree course.
After sequencing of the genome has been done, the first thing that comes to mind is "Where are the genes?". Genome annotation is the process of attaching information to the biological sequences. It is an active area of research and it would help scientists a lot to undergo with their wet lab projects once they know the coding parts of a genome.
Secondary Structure Prediction of proteins Vijay Hemmadi
Secondary structure prediction has been around for almost a quarter of a century. The early methods suffered from a lack of data. Predictions were performed on single sequences rather than families of homologous sequences, and there were relatively few known 3D structures from which to derive parameters. Probably the most famous early methods are those of Chou & Fasman, Garnier, Osguthorbe & Robson (GOR) and Lim. Although the authors originally claimed quite high accuracies (70-80 %), under careful examination, the methods were shown to be only between 56 and 60% accurate (see Kabsch & Sander, 1984 given below). An early problem in secondary structure prediction had been the inclusion of structures used to derive parameters in the set of structures used to assess the accuracy of the method.
Some good references on the subject:
Automated sequencing of genomes require automated gene assignment
Includes detection of open reading frames (ORFs)
Identification of the introns and exons
Gene prediction a very difficult problem in pattern recognition
Coding regions generally do not have conserved sequences
Much progress made with prokaryotic gene prediction
Eukaryotic genes more difficult to predict correctly
it contains the detail information about Dynamic programming, Knapsack problem, Forward / backward knapsack, Optimal Binary Search Tree (OBST), Traveling sales person problem(TSP) using dynamic programming
STS stands for sequence tagged site which is short DNA sequence, generally between 100 and 500 bp in length, that is easily recognizable and occurs only once in the chromosome or genome being studied.
Scoring system is a set of values for qualifying the set of one residue being substituted by another in an alignment.
It is also known as substitution matrix.
Scoring matrix of nucleotide is relatively simple.
A positive value or a high score is given for a match & negative value or a low score is given for a mismatch.
Scoring matrices for amino acids are more complicated because scoring has to reflect the physicochemical properties of amino acid residues.
Ab Initio Protein Structure Prediction is a method to determine the tertiary structure of protein in the absence of experimentally solved structure of a similar/homologous protein. This method builds protein structure guided by energy function.
I had prepared this presentation for an internal project during my masters degree course.
After sequencing of the genome has been done, the first thing that comes to mind is "Where are the genes?". Genome annotation is the process of attaching information to the biological sequences. It is an active area of research and it would help scientists a lot to undergo with their wet lab projects once they know the coding parts of a genome.
Secondary Structure Prediction of proteins Vijay Hemmadi
Secondary structure prediction has been around for almost a quarter of a century. The early methods suffered from a lack of data. Predictions were performed on single sequences rather than families of homologous sequences, and there were relatively few known 3D structures from which to derive parameters. Probably the most famous early methods are those of Chou & Fasman, Garnier, Osguthorbe & Robson (GOR) and Lim. Although the authors originally claimed quite high accuracies (70-80 %), under careful examination, the methods were shown to be only between 56 and 60% accurate (see Kabsch & Sander, 1984 given below). An early problem in secondary structure prediction had been the inclusion of structures used to derive parameters in the set of structures used to assess the accuracy of the method.
Some good references on the subject:
Automated sequencing of genomes require automated gene assignment
Includes detection of open reading frames (ORFs)
Identification of the introns and exons
Gene prediction a very difficult problem in pattern recognition
Coding regions generally do not have conserved sequences
Much progress made with prokaryotic gene prediction
Eukaryotic genes more difficult to predict correctly
it contains the detail information about Dynamic programming, Knapsack problem, Forward / backward knapsack, Optimal Binary Search Tree (OBST), Traveling sales person problem(TSP) using dynamic programming
Dynamic Programming is a method for solving a complex problem by breaking it down into a collection of simpler subproblems, solving each of those subproblems just once, and storing their solutions using a memory-based data structure (array, map,etc).
The Needleman–Wunsch algorithm is an algorithm used in bioinformatics to align protein or nucleotide sequences. The Needleman–Wunsch algorithm is still widely used for optimal global alignment, particularly when the quality of the global alignment is of the utmost importance.The algorithm essentially divides a large problem (e.g. the full sequence) into a series of smaller problems and uses the solutions to the smaller problems to reconstruct a solution to the larger problem. It is also sometimes referred to as the optimal matching algorithm and the global alignment technique.
https://telecombcn-dl.github.io/2018-dlai/
Deep learning technologies are at the core of the current revolution in artificial intelligence for multimedia data analysis. The convergence of large-scale annotated datasets and affordable GPU hardware has allowed the training of neural networks for data analysis tasks which were previously addressed with hand-crafted features. Architectures such as convolutional neural networks, recurrent neural networks or Q-nets for reinforcement learning have shaped a brand new scenario in signal processing. This course will cover the basic principles of deep learning from both an algorithmic and computational perspectives.
Global and local alignment (bioinformatics)Pritom Chaki
A general global alignment technique is the Needleman–Wunsch algorithm, which is based on dynamic programming. Local alignments are more useful for dissimilar sequences that are suspected to contain regions of similarity or similar sequence motifs within their larger sequence context.
Techniques to optimize the pagerank algorithm usually fall in two categories. One is to try reducing the work per iteration, and the other is to try reducing the number of iterations. These goals are often at odds with one another. Skipping computation on vertices which have already converged has the potential to save iteration time. Skipping in-identical vertices, with the same in-links, helps reduce duplicate computations and thus could help reduce iteration time. Road networks often have chains which can be short-circuited before pagerank computation to improve performance. Final ranks of chain nodes can be easily calculated. This could reduce both the iteration time, and the number of iterations. If a graph has no dangling nodes, pagerank of each strongly connected component can be computed in topological order. This could help reduce the iteration time, no. of iterations, and also enable multi-iteration concurrency in pagerank computation. The combination of all of the above methods is the STICD algorithm. [sticd] For dynamic graphs, unchanged components whose ranks are unaffected can be skipped altogether.
Programmed Assembly of Synthetic Protocells into Thermoresponsive PrototissuesZohaib HUSSAIN
Programmed assembly of synthetic protocells into thermoresponsive prototissues
Programmed assembly of synthetic protocells into thermoresponsive prototissues
Programmed assembly of synthetic protocells into thermoresponsive prototissues
Programmed assembly of synthetic protocells into thermoresponsive prototissues
Programmed assembly of synthetic protocells into thermoresponsive prototissues
Introduction
Anatomy and Physiology of bone
Bone Tissue Engineering
Recent studies related to bone tissue engineering
Commercialized products and ongoing clinical trials
Biomedical start-ups
Concluding remarks
Introduction
Anatomy and Physiology of bone
Bone Tissue Engineering
Recent studies related to bone tissue engineering
Commercialized products and ongoing clinical trials
Biomedical start-ups
Concluding remarks
Introduction
Anatomy and Physiology of bone
Bone Tissue Engineering
Recent studies related to bone tissue engineering
Commercialized products and ongoing clinical trials
Biomedical start-ups
Concluding remarks
Large-scale Production of Stem Cells Utilizing MicrocarriersZohaib HUSSAIN
Large-scale Production of Stem Cells Utilizing MicrocarriersLarge-scale Production of Stem Cells Utilizing MicrocarriersLarge-scale Production of Stem Cells Utilizing MicrocarriersLarge-scale Production of Stem Cells Utilizing MicrocarriersLarge-scale Production of Stem Cells Utilizing MicrocarriersLarge-scale Production of Stem Cells Utilizing MicrocarriersLarge-scale Production of Stem Cells Utilizing MicrocarriersLarge-scale Production of Stem Cells Utilizing MicrocarriersLarge-scale Production of Stem Cells Utilizing MicrocarriersLarge-scale Production of Stem Cells Utilizing Microcarriers
PHOTOSYNTHESIS: What we have learned so far? Zohaib HUSSAIN
No matter how complex or advanced a machine, such as the latest cellular phone, the device cannot function without energy. Living things, similar to machines, have many complex components; they too cannot do anything without energy, which is why humans and all other organisms must “eat” in some form or another. That may be common knowledge, but how many people realize that every bite of every meal ingested depends on the process of photosynthesis?
Contents
1. Insulin Molecule
2. Effect of Insulin in Body
3. History of Insulin
4. Recent Trends in Insulin Productions and Types
4.1 Animal Insulins
4.2 Long-Acting Insulins
4.3 Human Insulins
4.4 Insulin Analogues
4.5 Biosimilar Insulins
5. Insulin Production (Chain A and Chain B Method)
5.1 Upstream Processing
5.2 Downstream Processing
6. The Proinsulin Process
7. Insulin Available in Market with Different Brand Names
8. References
Oxidation & Reduction involves electron transfer & How enzymes find their sub...Zohaib HUSSAIN
Oxidation is loss of electrons
Reduction is gain of electrons
Oxidation is always accompanied by reduction
The total number of electrons is kept constant
Oxidizing agents oxidize and are themselves reduced
Reducing agents reduce and are themselves oxidized
Cellulase (Types, Sources, Mode of Action & Applications)Zohaib HUSSAIN
Cellulase is a class of enzyme that catalyzes the cellulolysis i.e., hydrolysis of cellulose. Celulase is a multiple enzyme system consisting of endo – 1, 4 –β–D – glucanases and exo – 1, 4 –β– D – glucanases along with cellobiase (β– D – glucosideglucano hydrolase).
Types of Cellulases
On the basis of fractionation studies on culture filtrate have demonstrated that, there are ‘three’ major types of enzymes involved in the hydrolysis of native cellulose to glucose, namely: Others are produced by the some animals and plants.
Amylases (Types, Sources, Mode of Action & Applications)Zohaib HUSSAIN
Amylases are important hydrolase enzymes which have been widely used since many decades. These enzymes randomly cleave internal glycosidic linkages in starch molecules to hydrolyze them and yield dextrins and oligosaccharides. Among amylases α-Amylase is in maximum demand due to its wide range of applications in the industrial front. α-Amylase can be produced by plant or microbial sources. The ubiquitous nature, ease of production and broad spectrum of applications make α-Amylase an industrially important enzyme.
Life on Earth (By Alonso Ricardo and Jack W. Szostak) Summary (By Zohaib Hus...Zohaib HUSSAIN
Life on Earth (By Alonso Ricardo and Jack W. Szostak)
Summary (By Zohaib Hussain)
Life on Earth (By Alonso Ricardo and Jack W. Szostak)
Summary (By Zohaib Hussain)
Life on Earth (By Alonso Ricardo and Jack W. Szostak)
Summary (By Zohaib Hussain)
Life on Earth (By Alonso Ricardo and Jack W. Szostak)
Summary (By Zohaib Hussain)
Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room Layout of the Cell Culture Room
1. Levels of gene regulation
The observation that differences in the RNA and protein content of different tissues are not paralleled by significant differences in their DNA content indicates that the process whereby DNA produces mRNA must be the level at which gene expression is regulated in eukaryotes. In bacteria this process involves only a single stage, that of transcription, in which RNA copy of the DNA is produced by the enzyme RNA polymerase. Even while this process is still occurring, ribosomes attach to the nascent RNA chain and begin to translate it into protein. Hence cases
of gene regulation in bacteria, such as the switching on of the synthesis of the enzyme β-galactosidase in response to the presence of lactose (its substrate), are mediated by increased transcription of the appropriate gene. Clearly, a similar regulation of gene transcription in different tissues, or in response to substances such as steroid hormones which induce the synthesis of new proteins, represents an attractive method of gene regulation in eukaryotes.
In contrast to the situation in bacteria, however, a number of stages intervene between the initial synthesis of the primary RNA transcript and the eventual production of mRNA (Fig. 1).
The initial transcript is modified at its 5′ end by the addition of a cap structure containing a modified guanosine residue and is subsequently cleaved near its 3′ end, followed by the addition of up to 200 adenosine residues in a process known as polyadenylation. Subsequently, intervening sequences or introns, which interrupt the protein-coding sequence in both the DNA and the primary transcript of many genes. Although this produces a functional mRNA, the spliced molecule must then be transported from the nucleus, where these processes occur, to the cytoplasm where it can be translated into protein.
Telomere, Functions & Role in Aging & CancerZohaib HUSSAIN
Why senescence occurs in eukaryotic organisms?
The major function of telomere is to cap the ends of chromosomes and protect the chromosomes from RED mechanism. As cells divide, telomeres continuously shorten with each successive cell division. Telomerase provides the necessary enzymatic activity to restore and maintain the telomere length. The vast majority of tumour's activate telomerase , and only few maintain telomeres by ALT mechanism relying on recombination. Telomere and telomerase are the attractive targets for anti-cancer therapeutics
Eukaryotic and Prokaryotic Chromosomes Eukaryotic and Prokaryotic Chromosomes Eukaryotic and Prokaryotic Chromosomes Eukaryotic and Prokaryotic Chromosomes Eukaryotic and Prokaryotic Chromosomes Eukaryotic and Prokaryotic Chromosomes Eukaryotic and Prokaryotic Chromosomes
Chromosomes are bundles of tightly coiled DNA located within the nucleus of almost every cell in our body. A chromosome is a DNA molecule with part or all of the genetic material (genome) of an organism. Chromosomes are normally visible under a light microscope only when the cell is undergoing the metaphase of cell division. Before this happens, every chromosome is copied once (S phase), and the copy is joined to the original by a centromere, resulting in an X-shaped structure. The original chromosome and the copy are now called sister chromatids. During metaphase, when a chromosome is in its most condensed state, the X-shape structure is called a metaphase chromosome.
"Impact of front-end architecture on development cost", Viktor TurskyiFwdays
I have heard many times that architecture is not important for the front-end. Also, many times I have seen how developers implement features on the front-end just following the standard rules for a framework and think that this is enough to successfully launch the project, and then the project fails. How to prevent this and what approach to choose? I have launched dozens of complex projects and during the talk we will analyze which approaches have worked for me and which have not.
Dev Dives: Train smarter, not harder – active learning and UiPath LLMs for do...UiPathCommunity
💥 Speed, accuracy, and scaling – discover the superpowers of GenAI in action with UiPath Document Understanding and Communications Mining™:
See how to accelerate model training and optimize model performance with active learning
Learn about the latest enhancements to out-of-the-box document processing – with little to no training required
Get an exclusive demo of the new family of UiPath LLMs – GenAI models specialized for processing different types of documents and messages
This is a hands-on session specifically designed for automation developers and AI enthusiasts seeking to enhance their knowledge in leveraging the latest intelligent document processing capabilities offered by UiPath.
Speakers:
👨🏫 Andras Palfi, Senior Product Manager, UiPath
👩🏫 Lenka Dulovicova, Product Program Manager, UiPath
Connector Corner: Automate dynamic content and events by pushing a buttonDianaGray10
Here is something new! In our next Connector Corner webinar, we will demonstrate how you can use a single workflow to:
Create a campaign using Mailchimp with merge tags/fields
Send an interactive Slack channel message (using buttons)
Have the message received by managers and peers along with a test email for review
But there’s more:
In a second workflow supporting the same use case, you’ll see:
Your campaign sent to target colleagues for approval
If the “Approve” button is clicked, a Jira/Zendesk ticket is created for the marketing design team
But—if the “Reject” button is pushed, colleagues will be alerted via Slack message
Join us to learn more about this new, human-in-the-loop capability, brought to you by Integration Service connectors.
And...
Speakers:
Akshay Agnihotri, Product Manager
Charlie Greenberg, Host
PHP Frameworks: I want to break free (IPC Berlin 2024)Ralf Eggert
In this presentation, we examine the challenges and limitations of relying too heavily on PHP frameworks in web development. We discuss the history of PHP and its frameworks to understand how this dependence has evolved. The focus will be on providing concrete tips and strategies to reduce reliance on these frameworks, based on real-world examples and practical considerations. The goal is to equip developers with the skills and knowledge to create more flexible and future-proof web applications. We'll explore the importance of maintaining autonomy in a rapidly changing tech landscape and how to make informed decisions in PHP development.
This talk is aimed at encouraging a more independent approach to using PHP frameworks, moving towards a more flexible and future-proof approach to PHP development.
Neuro-symbolic is not enough, we need neuro-*semantic*Frank van Harmelen
Neuro-symbolic (NeSy) AI is on the rise. However, simply machine learning on just any symbolic structure is not sufficient to really harvest the gains of NeSy. These will only be gained when the symbolic structures have an actual semantics. I give an operational definition of semantics as “predictable inference”.
All of this illustrated with link prediction over knowledge graphs, but the argument is general.
JMeter webinar - integration with InfluxDB and GrafanaRTTS
Watch this recorded webinar about real-time monitoring of application performance. See how to integrate Apache JMeter, the open-source leader in performance testing, with InfluxDB, the open-source time-series database, and Grafana, the open-source analytics and visualization application.
In this webinar, we will review the benefits of leveraging InfluxDB and Grafana when executing load tests and demonstrate how these tools are used to visualize performance metrics.
Length: 30 minutes
Session Overview
-------------------------------------------
During this webinar, we will cover the following topics while demonstrating the integrations of JMeter, InfluxDB and Grafana:
- What out-of-the-box solutions are available for real-time monitoring JMeter tests?
- What are the benefits of integrating InfluxDB and Grafana into the load testing stack?
- Which features are provided by Grafana?
- Demonstration of InfluxDB and Grafana using a practice web application
To view the webinar recording, go to:
https://www.rttsweb.com/jmeter-integration-webinar
Accelerate your Kubernetes clusters with Varnish CachingThijs Feryn
A presentation about the usage and availability of Varnish on Kubernetes. This talk explores the capabilities of Varnish caching and shows how to use the Varnish Helm chart to deploy it to Kubernetes.
This presentation was delivered at K8SUG Singapore. See https://feryn.eu/presentations/accelerate-your-kubernetes-clusters-with-varnish-caching-k8sug-singapore-28-2024 for more details.
UiPath Test Automation using UiPath Test Suite series, part 3DianaGray10
Welcome to UiPath Test Automation using UiPath Test Suite series part 3. In this session, we will cover desktop automation along with UI automation.
Topics covered:
UI automation Introduction,
UI automation Sample
Desktop automation flow
Pradeep Chinnala, Senior Consultant Automation Developer @WonderBotz and UiPath MVP
Deepak Rai, Automation Practice Lead, Boundaryless Group and UiPath MVP
State of ICS and IoT Cyber Threat Landscape Report 2024 previewPrayukth K V
The IoT and OT threat landscape report has been prepared by the Threat Research Team at Sectrio using data from Sectrio, cyber threat intelligence farming facilities spread across over 85 cities around the world. In addition, Sectrio also runs AI-based advanced threat and payload engagement facilities that serve as sinks to attract and engage sophisticated threat actors, and newer malware including new variants and latent threats that are at an earlier stage of development.
The latest edition of the OT/ICS and IoT security Threat Landscape Report 2024 also covers:
State of global ICS asset and network exposure
Sectoral targets and attacks as well as the cost of ransom
Global APT activity, AI usage, actor and tactic profiles, and implications
Rise in volumes of AI-powered cyberattacks
Major cyber events in 2024
Malware and malicious payload trends
Cyberattack types and targets
Vulnerability exploit attempts on CVEs
Attacks on counties – USA
Expansion of bot farms – how, where, and why
In-depth analysis of the cyber threat landscape across North America, South America, Europe, APAC, and the Middle East
Why are attacks on smart factories rising?
Cyber risk predictions
Axis of attacks – Europe
Systemic attacks in the Middle East
Download the full report from here:
https://sectrio.com/resources/ot-threat-landscape-reports/sectrio-releases-ot-ics-and-iot-security-threat-landscape-report-2024/
The Art of the Pitch: WordPress Relationships and SalesLaura Byrne
Clients don’t know what they don’t know. What web solutions are right for them? How does WordPress come into the picture? How do you make sure you understand scope and timeline? What do you do if sometime changes?
All these questions and more will be explored as we talk about matching clients’ needs with what your agency offers without pulling teeth or pulling your hair out. Practical tips, and strategies for successful relationship building that leads to closing the deal.
2. Alignment
used to uncover homologies between sequences
combined with phylogenetic studies
can determine orthologous and paralogous
relationships
Global Alignments
compares one whole sequence with other entire
sequence
computationally expensive
Local Alignment
uses a subset of a sequence and attempts to align it
to subset of other sequences
computationally less expensive
3. Dynamic Programming:
dynamic programing is solving complex
prblems by breaking them into a simpler
subproblems.
Problem can be divided into many smaller
parts.
Needleman and Wunsch were the first to
propose this method.
4. Needleman and Wunsch describes general
algorithm for sequence aignment.
Maximize a score of similarity to give maximun
match.
Maximun match= largest number of nucleotides
that can be match with others.
That want to quantify sequence similarity
between two sequences.
5. Dynamic programming in bioinformatics
Dynamic programming is widely used in
bioinformatics for the tasks such as sequence
alignment, protein folding, RNA structure
prediction and protein-DNA binding.
First dynamic programming algorithms for
protein-DNA binding were developed in the 1970s
independently by Charles Delisi in USA
and Georgii Gurskii and Alexanderr
zasedatelev in USSR.
6. Dynamic Programming in sequence alignment
There are three steps in dynamic programing.
1. initialization.
The first step in the global alignment dynamic programming
approach is to create a matrix with M + 1 columns and N + 1
rows where M and N correspond to the size of the sequences to
be aligned.
2. Matrix filling(scoring)
We fill the matrix with highest possible score.
To align with diagnol ( align in next position.)
Allign in off-diagonal requires inserion of crossponding gaps
3. Traceback and aligning
Move from last corner and follow arrow.
7. Global alignment via dynamic programing
1st column and 1st row will be empty.
Fill 1st block with zero
Then fill 1st row and 1st coulmn with gap penality multiples.
While filling the matrix there are three possible values
horizental: score+ gap penality
Verticle: score+ gap penality
Diagonal: score+(match/mismatch)
We have to write max score from these values in a
cell
Let ,
match = + 1
mismatch= -1
gap penality= -2
9. A A T C
0 -2 -4 -6 -8
A -2
( 1) ( -4)
1
(-4)
-1 -6
-1
-1
-3 -5
G -4
-1 0 -2 -4
C -6
-3 -2 -1 -1
10. Backward tracking
In backward tracking we have to move
from last cell( lower corner) and follows
arrow from which cell the current cell’s
values come from and go ahead.
11. A A T C
0 -2 -4 -6 -8
A -2 1 -1 -3 -5
G -4
-1 0 -2 -4
C -6
-3 -2 -1 -1
12. A A T C
0 -2 -4 -6 -8
A -2 1 -1 -3 -5
G -4
-1 0 -2 -4
C -6
-3 -2 -1 -1
Path 1
Path 2
13. Backtracking
Now we have to allign this sequence.
For alligning there are 2 rules.
1. If the value come from column we will have
to write two sequences
2. If value come from horizontal or vertical
then we will have to write perpendicular
and add gap to other side.
14. Backtracking
Here we have two paths. So we will get two
possible sequences.
We will write sequence from 3’-end.
Path 1:
Seq#1 A A T C
Seq#2 - A G C
16. Local alignment via dynamic programing
Algorithim is same as in global alignment,
but there are some changes.
We fill 1st column and 1st row with zero.
If the value comes in negative number than
it is replaced by zero.
Backtracking will be start from maximun
value.
18. G A A T T C A G T T A
0 0 0 0 0 0 0 0 0 0 0 0
G 0 1 1 1 1 1 1 1 1 1 1 1
G 0 1 1 1 1 1 1 1 2 2 2 2
A 0 1 2 2 2 2 2 2 2 2 2 3
T 0 1 2 2 3 3 3 3 3 3 3 3
C 0 1 2 2 3 3 4 4 4 4 4 4
G 0 1 2 2 3 3 4 4 5 5 5 5
A 0 1 2 3 3 3 3 4 5 5 5 6
19. Bactracking
After the matrix fill step, the maximum alignment
score for the two test sequences is 6. The traceback
step determines the actual alignment(s) that result
in the maximum score.
20. G A A T T C A G T T A
0 0 0 0 0 0 0 0 0 0 0 0
G 0 1 1 1 1 1 1 1 1 1 1 1
G 0 1 1 1 1 1 1 1 2 2 2 2
A 0 1 2 2 2 2 2 2 2 2 2 3
T 0 1 2 2 3 3 3 3 3 3 3 3
C 0 1 2 2 3 3 4 4 4 4 4 4
G 0 1 2 2 3 3 4 4 5 5 5 5
A 0 1 2 3 3 3 3 4 5 5 5 6
21. Backtracking
Rule will be same for this as in global
alignment
Sequence alignment :
Seq#1 G A A T T C A G T TA
Seq#2 G A - T C – G - - A
So in this way we align the sequence using
dynamic programing.