SEQanswers - Threads Tagged with variant analysis

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Threads Tagged with variant analysis

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Threads Tagged with variant analysis
	Thread / Thread Starter	Last Post	Replies	Views	Forum
	get rsID or positions from variant name/gene info floydian_slip	11-10-2020 06:04 AM by floydian_slip	0	612	Bioinformatics
	Webinar: Perform large NGS assembly and analysis on any computer DNASTAR	03-14-2019 07:56 AM by DNASTAR	0	2,279	Events / Conferences
	Adding GT tag to Strelka Output erichpeterson	08-09-2018 09:33 AM by GobiJerboa	1	6,752	Genomic Resequencing
	Variant Analysis, Bioinformatics Prerequisites, & Genome Browser workshops @ UC Davis najoshi	07-12-2018 06:08 PM by najoshi	0	2,127	Events / Conferences
	Training in Variant Analysis @NIH,USA Feb 27 - Mar 2, 2018 aabi	01-09-2018 11:58 PM by aabi	0	2,305	Events / Conferences
	Webinar on Analysis of Variants using GeneSpring GX 14.9 on 6 Dec 2017 Strandlife	11-27-2017 01:31 AM by Strandlife	1	9,022	Webinar Series
	Variant Analysis Workshop, Aug. 21-25 mbritton	06-13-2017 12:25 PM by mbritton	0	2,236	Events / Conferences
	Haplotyping/genotyping tool PacBio? BioGenomics	04-05-2017 03:14 AM by BioGenomics	2	1,874	Pacific Biosciences
	RNA-Seq and Variant Analysis Workshop (Aug 29 - Sep 2) mbritton	07-25-2016 12:12 PM by mbritton	0	2,063	Events / Conferences
	Webinar 6/22: Speed, Accuracy and Capacity for Your NGS Analysis Projects DNASTAR	06-21-2016 08:27 AM by DNASTAR	0	1,744	Events / Conferences
	Webinar: Variant Analysis in Lasergene Genomics Suite DNASTAR	03-16-2016 10:17 AM by DNASTAR	0	1,626	Events / Conferences
	Error: Invalid format for pileup at line null in varscan2 dena.dinesh	12-14-2015 08:27 AM by RobUK	1	1,827	Bioinformatics
	variant calling on a subsample of a BAM file.. batman	11-11-2015 12:23 AM by dpryan	5	2,003	Bioinformatics
	Webinar: Achieving Highly Accurate NGS Variant Calling DNASTAR	10-20-2015 06:41 AM by DNASTAR	0	1,797	Events / Conferences
	Error using vcf-stats ruchi1621	04-17-2015 05:20 AM by Nnogueira	3	2,631	Bioinformatics
	ANNOVAR Results Analysis arcolombo698	04-25-2014 10:36 PM by arcolombo698	0	1,262	RNA Sequencing
	Homopolymer expansion variants hbeale	04-13-2014 03:00 PM by gringer	1	1,829	Bioinformatics
	Rare variants from annotated vcf file rohan_1925	02-11-2014 01:35 PM by m_two	2	2,051	Bioinformatics
	How to analyze your own exome Knaus	01-09-2014 05:47 AM by Knaus	3	10,867	Personalized Genomics
	PLoS One: Filtering for Compound Heterozygous Sequence Variants at GeneTalk Knaus	12-13-2013 02:16 AM by Knaus	1	3,206	Literature Watch
	vcf-compare output bruce01	10-15-2013 03:59 PM by bruce01	0	4,174	Bioinformatics
	Filter variants by DP4 (total)? Genomics101	09-23-2013 10:46 AM by Genomics101	2	2,114	Bioinformatics
	Options for PGM Variant Analysis HeidiJTP	06-29-2013 09:02 PM by nilshomer	9	6,843	Ion Torrent
	RUbioSeq: a suite of parallelized pipelines for exome variation, CNVs and Bis-Seq gonvader	05-01-2013 12:58 PM by gonvader	0	2,089	Literature Watch
	Number of variants from mouse exome looks very small Shingo	04-03-2013 05:53 PM by Shingo	2	2,185	Genomic Resequencing
	Illumina Truseq Exome 62Mb - variant metrics? chongm	03-06-2013 12:25 AM by chongm	0	1,488	Bioinformatics
	NGS data: append annotations from HGMD lsantome	02-20-2013 03:00 AM by Aquarius	3	2,034	Bioinformatics
	Detecting SNPs, SNVs using CLC genomics wqorkbench NGS_New_User	10-10-2012 07:20 AM by NGS_New_User	0	3,000	Bioinformatics
	False negative variant calling in haploids. Call variants using coverage (not stats)? Genomics101	06-07-2012 12:29 PM by BAMseek	3	3,083	Bioinformatics
	Complete Genomics Variant Calls quicksand21	10-11-2011 08:21 AM by karenliu	2	3,590	Bioinformatics

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