SEQanswers - Threads Tagged with variant analysis

		SEQanswers > Tags
Threads Tagged with variant analysis

Page 1 of 2

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 05:04 AM by floydian_slip	0	1,230	Bioinformatics
	Webinar: Perform large NGS assembly and analysis on any computer DNASTAR	03-14-2019 06:56 AM by DNASTAR	0	3,225	Events / Conferences
	Adding GT tag to Strelka Output erichpeterson	08-09-2018 08:33 AM by GobiJerboa	1	10,004	Genomic Resequencing
	Variant Analysis, Bioinformatics Prerequisites, & Genome Browser workshops @ UC Davis najoshi	07-12-2018 05:08 PM by najoshi	0	2,608	Events / Conferences
	Training in Variant Analysis @NIH,USA Feb 27 - Mar 2, 2018 aabi	01-09-2018 10:58 PM by aabi	0	2,849	Events / Conferences
	Webinar on Analysis of Variants using GeneSpring GX 14.9 on 6 Dec 2017 Strandlife	11-27-2017 12:31 AM by Strandlife	1	11,904	Webinar Series
	Variant Analysis Workshop, Aug. 21-25 mbritton	06-13-2017 11:25 AM by mbritton	0	2,545	Events / Conferences
	Haplotyping/genotyping tool PacBio? BioGenomics	04-05-2017 02:14 AM by BioGenomics	2	2,327	Pacific Biosciences
	RNA-Seq and Variant Analysis Workshop (Aug 29 - Sep 2) mbritton	07-25-2016 11:12 AM by mbritton	0	2,409	Events / Conferences
	Webinar 6/22: Speed, Accuracy and Capacity for Your NGS Analysis Projects DNASTAR	06-21-2016 07:27 AM by DNASTAR	0	2,398	Events / Conferences
	Webinar: Variant Analysis in Lasergene Genomics Suite DNASTAR	03-16-2016 09:17 AM by DNASTAR	0	1,964	Events / Conferences
	Error: Invalid format for pileup at line null in varscan2 dena.dinesh	12-14-2015 07:27 AM by RobUK	1	2,192	Bioinformatics
	variant calling on a subsample of a BAM file.. batman	11-10-2015 11:23 PM by dpryan	5	2,478	Bioinformatics
	Webinar: Achieving Highly Accurate NGS Variant Calling DNASTAR	10-20-2015 05:41 AM by DNASTAR	0	2,278	Events / Conferences
	Error using vcf-stats ruchi1621	04-17-2015 04:20 AM by Nnogueira	3	3,052	Bioinformatics
	ANNOVAR Results Analysis arcolombo698	04-25-2014 09:36 PM by arcolombo698	0	1,489	RNA Sequencing
	Homopolymer expansion variants hbeale	04-13-2014 02:00 PM by gringer	1	2,198	Bioinformatics
	Rare variants from annotated vcf file rohan_1925	02-11-2014 12:35 PM by m_two	2	2,519	Bioinformatics
	How to analyze your own exome Knaus	01-09-2014 04:47 AM by Knaus	3	13,763	Personalized Genomics
	PLoS One: Filtering for Compound Heterozygous Sequence Variants at GeneTalk Knaus	12-13-2013 01:16 AM by Knaus	1	3,647	Literature Watch
	vcf-compare output bruce01	10-15-2013 02:59 PM by bruce01	0	4,676	Bioinformatics
	Filter variants by DP4 (total)? Genomics101	09-23-2013 09:46 AM by Genomics101	2	2,555	Bioinformatics
	Options for PGM Variant Analysis HeidiJTP	06-29-2013 08:02 PM by nilshomer	9	7,480	Ion Torrent
	RUbioSeq: a suite of parallelized pipelines for exome variation, CNVs and Bis-Seq gonvader	05-01-2013 11:58 AM by gonvader	0	2,446	Literature Watch
	Number of variants from mouse exome looks very small Shingo	04-03-2013 04:53 PM by Shingo	2	2,617	Genomic Resequencing
	Illumina Truseq Exome 62Mb - variant metrics? chongm	03-05-2013 11:25 PM by chongm	0	1,903	Bioinformatics
	NGS data: append annotations from HGMD lsantome	02-20-2013 02:00 AM by Aquarius	3	2,370	Bioinformatics
	Detecting SNPs, SNVs using CLC genomics wqorkbench NGS_New_User	10-10-2012 06:20 AM by NGS_New_User	0	3,584	Bioinformatics
	False negative variant calling in haploids. Call variants using coverage (not stats)? Genomics101	06-07-2012 11:29 AM by BAMseek	3	3,623	Bioinformatics
	Complete Genomics Variant Calls quicksand21	10-11-2011 07:21 AM by karenliu	2	4,193	Bioinformatics

Page 1 of 2

All times are GMT -8. The time now is 02:44 AM.