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Thread | Thread Starter | Forum | Replies | Last Post |
Variants called using GATK from samples of Nextera and TruSeq exome enrichment kits | bioinf newbie | Illumina/Solexa | 1 | 11-01-2016 05:00 AM |
Almost all locations are called by samtools from RNA-seq data | Younghoon Kim | Bioinformatics | 2 | 05-09-2014 12:13 AM |
Too many Variants called by HaplotypeCaller GATK | drmaly | Bioinformatics | 2 | 12-05-2013 09:56 PM |
validated data | cmccabe | Ion Torrent | 0 | 04-29-2013 03:09 PM |
Pileup shows variants - Not called as SNPs | BertieWooster | Bioinformatics | 10 | 05-12-2011 11:57 AM |
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#1 |
Junior Member
Location: California Join Date: May 2017
Posts: 1
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I'm looking to develop methods to improve variant calling accuracy. I need an open dataset with the reads. Pre-aligned data such as with pileup files are ok.
I would need the variants contained in the reads to be validated by some gold standard. (perhaps with Sanger?) Is there such a dataset available to the public? |
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#2 |
Senior Member
Location: bethesda Join Date: Feb 2009
Posts: 700
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Check out "Genome in a Bottle" :
https://github.com/genome-in-a-bottle/giab_FAQ |
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