SEQanswers - Threads Tagged with variant calling

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Threads Tagged with variant calling

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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	01-19-2022 04:14 AM by uhrigs	9	7,682	Bioinformatics
	snpeff effect annotation confusion najoshi	07-07-2021 01:38 AM by najoshi	0	1,447	Bioinformatics
	Mutational Analysis: Identifying SNVs on demand thezgabby	05-10-2021 09:49 AM by thezgabby	0	12,724	Genomic Resequencing
	calling SNVs in shallow WGS data from liquid biopsy dnya	07-26-2020 11:10 PM by dnya	0	1,680	Bioinformatics
	How can unique molecular identifiers (UMIs) help to reduce quantitative biases? ecSeq Bioinformatics	06-04-2019 03:27 AM by ecSeq Bioinformatics	2	2,137	Bioinformatics
	Variant calling on matched primary and metastatic tumor without normal samples. RTM	03-26-2019 02:01 AM by RTM	0	2,174	Bioinformatics
	Adding GT tag to Strelka Output erichpeterson	08-09-2018 08:33 AM by GobiJerboa	1	9,976	Genomic Resequencing
	Webinar-Diagnosis of Rare Diseases using NGS Based Multi-gene Testing-Case studies Strandlife	04-24-2018 11:12 PM by Strandlife	2	2,758	Bioinformatics
	Variant calling using CRISP Aristotle	04-05-2018 03:30 AM by Aristotle	0	1,988	General
	Live Webinar on UMI-powered Ultra-sensitive Variant Calling on 13 Dec 2017 Strandlife	12-12-2017 09:43 PM by Strandlife	2	3,037	Bioinformatics
	False variant calls due to alignment (Allele specific expression, aka ASE) Sergio.pv	11-08-2017 05:22 AM by Sergio.pv	0	1,737	Bioinformatics
	Correct way of merging samples for father, mother, child trio variant calling Eurioste	07-05-2017 08:01 PM by finswimmer	1	3,138	Bioinformatics
	Live Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017 Strandlife	05-16-2017 01:51 AM by Strandlife	2	3,407	General
	Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017 Strandlife	04-17-2017 03:05 AM by Strandlife	0	2,774	Bioinformatics
	variant calling from pacBio Sequel data splaisan	03-25-2017 06:20 AM by splaisan	0	3,623	Bioinformatics
	Viral Genomics and Bioinformatics course August 2017, Glasgow rjorton	02-07-2017 03:25 PM by rjorton	0	3,584	Events / Conferences
	Question regarding Zygosity variant calling interpretation - homozygote variants NGS_New_User	11-21-2016 07:29 AM by NGS_New_User	0	8,252	De novo discovery
	Variants called using GATK from samples of Nextera and TruSeq exome enrichment kits bioinf newbie	11-01-2016 04:00 AM by HESmith	1	2,697	Illumina/Solexa
	Germline variant calling using tumor-normal pairs in GATK ty23991	07-05-2016 11:02 AM by ty23991	5	3,137	Bioinformatics
	picardtools LiftoverVcf losing majority of information lstbl	06-23-2016 10:19 AM by lstbl	0	1,496	Bioinformatics
	Illumina Truseq Pair end c_ro87	11-30-2015 10:59 AM by c_ro87	0	2,983	Bioinformatics
	Setting Up Variant Frequencies in TVC hanco	10-19-2015 05:21 PM by hanco	0	2,588	Ion Torrent
	FamSeq vs Polymutt vs DeNovoGear Kath	10-04-2015 02:53 PM by Len Trigg	3	4,507	Bioinformatics
	Normalization by the library size during variant detection NikTuzov	07-17-2015 06:24 AM by NikTuzov	2	3,479	Bioinformatics
	vcf from bam file frymor	06-26-2015 07:59 AM by SNPsaurus	4	10,229	Bioinformatics
	de novo assembly with de Bruijn colored graphs ArtificialBreeze	06-15-2015 12:26 PM by ArtificialBreeze	2	2,067	Bioinformatics
	Identifying variants in mitochondria normal/tumor pairs ramiro2k	05-20-2015 11:07 AM by ramiro2k	0	1,861	Bioinformatics
	Minimal coverage for accurate variant calling according to Illumina FDA submission? alunem	05-05-2015 04:42 AM by alunem	5	2,788	Illumina/Solexa
	variant calling in plant sfh838t	03-02-2015 11:54 AM by sfh838t	10	3,286	General
	Do variant callers miss rare variants in reference? [Super Explanatory Image Inside] Nikvailo	02-18-2015 01:58 AM by dariober	8	3,408	Bioinformatics

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