SEQanswers - Threads Tagged with variant calling

		SEQanswers > Tags
Threads Tagged with variant calling

Page 1 of 3

Threads Tagged with variant calling
	Thread / Thread Starter	Last Post	Replies	Views	Forum
	Arriba: Fast and accurate gene fusion detection from RNA-Seq data uhrigs	11-12-2020 08:41 AM by uhrigs	4	4,229	Bioinformatics
	calling SNVs in shallow WGS data from liquid biopsy dnya	07-27-2020 12:10 AM by dnya	0	722	Bioinformatics
	How can unique molecular identifiers (UMIs) help to reduce quantitative biases? ecSeq Bioinformatics	06-04-2019 04:27 AM by ecSeq Bioinformatics	2	1,429	Bioinformatics
	Variant calling on matched primary and metastatic tumor without normal samples. RTM	03-26-2019 03:01 AM by RTM	0	1,326	Bioinformatics
	Adding GT tag to Strelka Output erichpeterson	08-09-2018 09:33 AM by GobiJerboa	1	6,422	Genomic Resequencing
	Webinar-Diagnosis of Rare Diseases using NGS Based Multi-gene Testing-Case studies Strandlife	04-25-2018 12:12 AM by Strandlife	2	2,090	Bioinformatics
	Variant calling using CRISP Aristotle	04-05-2018 04:30 AM by Aristotle	0	1,391	General
	Live Webinar on UMI-powered Ultra-sensitive Variant Calling on 13 Dec 2017 Strandlife	12-12-2017 10:43 PM by Strandlife	2	2,246	Bioinformatics
	False variant calls due to alignment (Allele specific expression, aka ASE) Sergio.pv	11-08-2017 06:22 AM by Sergio.pv	0	1,191	Bioinformatics
	Correct way of merging samples for father, mother, child trio variant calling Eurioste	07-05-2017 09:01 PM by finswimmer	1	2,178	Bioinformatics
	Live Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017 Strandlife	05-16-2017 02:51 AM by Strandlife	2	2,494	General
	Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017 Strandlife	04-17-2017 04:05 AM by Strandlife	0	1,835	Bioinformatics
	variant calling from pacBio Sequel data splaisan	03-25-2017 07:20 AM by splaisan	0	2,797	Bioinformatics
	Viral Genomics and Bioinformatics course August 2017, Glasgow rjorton	02-07-2017 04:25 PM by rjorton	0	2,640	Events / Conferences
	Question regarding Zygosity variant calling interpretation - homozygote variants NGS_New_User	11-21-2016 08:29 AM by NGS_New_User	0	5,342	De novo discovery
	Variants called using GATK from samples of Nextera and TruSeq exome enrichment kits bioinf newbie	11-01-2016 05:00 AM by HESmith	1	1,937	Illumina/Solexa
	Germline variant calling using tumor-normal pairs in GATK ty23991	07-05-2016 12:02 PM by ty23991	5	2,326	Bioinformatics
	picardtools LiftoverVcf losing majority of information lstbl	06-23-2016 11:19 AM by lstbl	0	951	Bioinformatics
	Illumina Truseq Pair end c_ro87	11-30-2015 11:59 AM by c_ro87	0	2,200	Bioinformatics
	Setting Up Variant Frequencies in TVC hanco	10-19-2015 06:21 PM by hanco	0	2,051	Ion Torrent
	FamSeq vs Polymutt vs DeNovoGear Kath	10-04-2015 03:53 PM by Len Trigg	3	3,801	Bioinformatics
	Normalization by the library size during variant detection NikTuzov	07-17-2015 07:24 AM by NikTuzov	2	2,540	Bioinformatics
	vcf from bam file frymor	06-26-2015 08:59 AM by SNPsaurus	4	3,902	Bioinformatics
	de novo assembly with de Bruijn colored graphs ArtificialBreeze	06-15-2015 01:26 PM by ArtificialBreeze	2	1,387	Bioinformatics
	Identifying variants in mitochondria normal/tumor pairs ramiro2k	05-20-2015 12:07 PM by ramiro2k	0	1,306	Bioinformatics
	Minimal coverage for accurate variant calling according to Illumina FDA submission? alunem	05-05-2015 05:42 AM by alunem	5	2,147	Illumina/Solexa
	variant calling in plant sfh838t	03-02-2015 12:54 PM by sfh838t	10	2,618	General
	Do variant callers miss rare variants in reference? [Super Explanatory Image Inside] Nikvailo	02-18-2015 02:58 AM by dariober	8	2,531	Bioinformatics
	bam-readcount warning balthasar	12-19-2014 01:15 AM by balthasar	1	3,510	Bioinformatics
	Strelka: Somatic small-variant calling workflow for matched tumor-normal samples ctsa	12-15-2014 02:38 AM by Jane M	15	9,160	Bioinformatics

Page 1 of 3

All times are GMT -8. The time now is 09:17 PM.