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Thread | Thread Starter | Forum | Replies | Last Post |
NEWBIE: What is relation between SNP calling, INDEL calling and Genotype calling? | arkilis | Bioinformatics | 4 | 10-01-2013 06:57 PM |
De novo SNP calling in absence of complete reference assembly | fcr | De novo discovery | 15 | 09-21-2012 03:34 AM |
How to differentiate driver mutations from common/random mutations and SNPs in cancer | kumardeep | RNA Sequencing | 0 | 09-04-2012 02:51 AM |
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#1 |
Member
Location: Sydney Join Date: Jun 2013
Posts: 15
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Hi all,
Is anybody familiar with calling de novo mutations from whole genome sequences of parent-offspring trios (computationally) ? I have read that samtools and VarScan can do this but I would like to hear everyones experiences. ![]() Cheers! |
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#2 |
Member
Location: Switzerland Join Date: May 2013
Posts: 20
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What about Golden Helix Genome Browser?
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