Whole genome sequence for cancer
The sequencing principles of common sequencing instruments on the market: (1) first, construct a DNA template library. Obtain DNA library fragments (tens to hundreds of bases in length) by randomly breaking genomic DNA, or construct paired-end fragments that control the distance distribution. Adapter sequences were ligated to both ends of the DNA fragment and then denatured to obtain a single-stranded template library and immobilized on a solid surface. (2) Second, amplify the clones, which performed by one of several methods, such as bridge PCR and emulsion PCR. (3) Then, forming DNA clusters or amplifying microspheres of DNA cluster arrays on a chip, performing a series of cyclic reaction operations using a polymerase\ or ligase, and monitoring the optical events generated in each cycle biochemical reaction by a microscopic detection system. Time series analysis of the resulting array images is performed to obtain sequences of DNA fragments. These fragments are then assembled into longer contigs according to certain computer algorithms. Creative Biolabs uses the advanced SuPrecision™ platform to support researchers all over the world with their sequencing needs for cancer.www.creative-biolabs.com/suprecision
Whole genome sequence for cancer
The sequencing principles of common sequencing instruments on the market: (1) first, construct a DNA template library. Obtain DNA library fragments (tens to hundreds of bases in length) by randomly breaking genomic DNA, or construct paired-end fragments that control the distance distribution. Adapter sequences were ligated to both ends of the DNA fragment and then denatured to obtain a single-stranded template library and immobilized on a solid surface. (2) Second, amplify the clones, which performed by one of several methods, such as bridge PCR and emulsion PCR. (3) Then, forming DNA clusters or amplifying microspheres of DNA cluster arrays on a chip, performing a series of cyclic reaction operations using a polymerase\ or ligase, and monitoring the optical events generated in each cycle biochemical reaction by a microscopic detection system. Time series analysis of the resulting array images is performed to obtain sequences of DNA fragments. These fragments are then assembled into longer contigs according to certain computer algorithms. Creative Biolabs uses the advanced SuPrecision™ platform to support researchers all over the world with their sequencing needs for cancer.www.creative-biolabs.com/suprecision
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Whole genome sequence for cancer
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- 20. WGS WorkFlow 1 2 WHOLE GENOME SEQUENCING FOR CANCER Creative Biolabs Whole Genome Sequencing Service for Cancer Applications © 2007 - 2019 Creative-Biolabs All Rights Reserved Email: info@creative-biolabs.com Tel: 1-631-381-2994 FEATURES: WHAT WE DO: Whole Exome Sequencing (WES) Service Target Sequencing Service Whole Transcriptome Sequencing (WTS) Service Immune Repertoire Sequencing Service Up to 99.99% Accuracy Identify Potential Causative Variants Detect DNA Modifications without Bisulfite Treatment Identify Large Structural Variants Phase Alleles and Ariants
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