|
|
|
|
|||||||
Similar Threads
|
||||
| Thread | Thread Starter | Forum | Replies | Last Post |
| RTG 3.5: Somatic calling / metagenomics / variant comparison / BSD Licensing | Len Trigg | Vendor Forum | 2 | 10-15-2015 06:33 PM |
| Strelka: Somatic small-variant calling workflow for matched tumor-normal samples | ctsa | Bioinformatics | 15 | 12-15-2014 02:38 AM |
| Looking for tools for calling snv and indel(Somatic Variant) | fabrice | Bioinformatics | 1 | 06-13-2014 11:29 AM |
| Tolerances for non cells-of-interest for somatic variant calling | rjohnp | Sample Prep / Library Generation | 0 | 04-04-2013 09:16 AM |
| Variant Calling from paired end RNAseq data | ron128 | Bioinformatics | 2 | 03-30-2013 01:33 AM |
 |
|
|
Thread Tools |
02-09-2016, 01:48 PM
|
#1 |
|
Junior Member
Location: USA Join Date: Feb 2016
Posts: 2
|
[deleted][deleted][deleted][deleted][deleted][deleted]
[deleted][deleted][deleted][deleted][deleted][deleted]
Last edited by umn_bist; 05-02-2016 at 11:52 PM. |
|
|
|
| Thread Tools | |
|
|
