Postdoctoral Fellowship: Computational biology of ICGC pan-cancer genomes – integrative data analysis of cancer genome and polyomic datasets
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Strelka: Somatic small-variant calling workflow for matched tumor-normal samples
Hello All,
Strelka is a new workflow available to call SNVs and small indels from sequencing data for matched tumor-normal samples. It...
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Cancer Genomics Advice
Dear All,
I am a bit of a novice when it come to bioinformatics so please do no condemn my current ignorance. I am a first year PhD student...
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CNANorm: A normalization method for Copy Number Aberration in cancer samples.
CNAnorm performs ratio, GC content correction and normalization of data obtained using low coverage (one read every 100-10,000 bp) high throughput sequencing....Last edited by stefanoberri; 11-18-2011, 03:11 AM.
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Innovative Solutions for Targeted Amplification in Next-Generation Sequencing
Talk at Drug Discovery & Diagnostic Development Week
Hyatt Regency San Francisco
Wednesday, Aug. 3
2:30pm - 3:00pm
ht...
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mapping of breakpoint
I have run some Illumina paired end and Illumina mate pair experiments, to analyze for chromosomal rearrangements in cancer genomics.
What...
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Cancer Genomics using Illumina GA
Hi All
We recently have run cancer samples on Illumina. As this is our first such run, I wanted to know the tools out there to process/analyze...