Genomic Resequencing

		SEQanswers > Applications Forums
Genomic Resequencing

Page 1 of 10

Last »

Threads in Forum : Genomic Resequencing

Forum Tools

Search this Forum

Rating Thread / Thread Starter	Last Post	Replies	Views
What are the applications of CRISPR Based Microbe Genome Editing Service wendywilson	10-27-2020 01:39 AM by wendywilson	0	889
Find SNPs in related strains dsybers	10-09-2019 09:45 AM by dsybers	0	8,922
How to estimate genetic variation in a population with RNASeq data? dacotahm	09-26-2019 09:01 AM by dacotahm	0	2,411
Problem in mpileup file where size of sequence does not match size of quality cryptodice	08-04-2019 08:16 PM by cryptodice	0	3,356
Reliability of short insert sizes lburmz	05-14-2019 01:57 AM by lburmz	0	3,558
Variant and Genotype calling Alex_Dor	04-12-2019 06:22 AM by Alex_Dor	0	3,346
SNP calling on samples sequenced with different technology weehzer	09-10-2018 04:49 AM by weehzer	0	6,699
Calculate probability of a given sequence _anli	08-23-2018 09:24 AM by _anli	0	4,148
PL high support for each GT for all SNPS htetre	08-20-2018 12:05 PM by htetre	2	4,361
Experiences with SeqCap EZ Prime j_he	08-16-2018 04:29 PM by j_he	0	3,995
Adding GT tag to Strelka Output erichpeterson	08-09-2018 09:33 AM by GobiJerboa	1	6,405
The R-square between coverage and short variants number Chen-Tau Lin	07-31-2018 08:59 PM by Chen-Tau Lin	0	3,871
Control sample for human germline SNP discovery? whe	07-15-2018 07:11 PM by whe	0	4,357
SureSelect XT Probes icahn_seq	02-04-2018 09:28 AM by icahn_seq	2	6,450
SNPs at Interval Boundaries in GATK HaplotypeCaller peterlchang	10-24-2017 02:53 PM by peterlchang	0	5,840
Chromosomal translocation, which NGS method appropriate deepbiomed	09-13-2017 07:09 AM by r.rosati	4	6,669
mpileup only calling snps for chr1 not entire genome htetre	06-20-2017 02:56 PM by htetre	1	4,950
Finding two strains of a genome having SNPs/SNVs in their repeat regions smh.oloomi	06-10-2017 09:52 PM by smh.oloomi	0	4,855
Calling variants when mapping reads from different species than reference gruberjd	05-19-2017 12:52 PM by Brian Bushnell	3	6,355
Panel Validation using NA12878 DNA NielQC	05-05-2017 04:36 AM by NielQC	0	5,501
How to generate VCF from HISAT2 pre-built SNP index? jol.espinoz	04-30-2017 12:03 PM by jol.espinoz	0	6,315
Somatic Mutation Amount cindylanzao	04-23-2017 06:02 PM by cindylanzao	0	4,986
Coverage of reads not homogenous (sureselect target enrichement) Sam64	04-14-2017 09:37 AM by czhang	2	6,927
Removing duplicate PacBio reads AgatheJ	02-19-2017 09:38 AM by AgatheJ	8	7,564
CONTRA cnv on chrX Michel Meyer	02-06-2017 09:00 AM by Michel Meyer	0	4,920
hope to know the softwares to plot this image about genomic linkage map zhdorothy	12-12-2016 07:22 PM by zhdorothy	0	5,835
fastq.gz size for human WGS coverage calculation yipukangda	11-08-2016 06:26 PM by yipukangda	2	6,596
Abnormaly amount of reads Mr.Zurich1992	10-02-2016 03:44 AM by dpryan	1	5,558
Illumina vs. Agilent Exome enrichment - higher false positive rates markusl	09-22-2016 08:22 AM by Geneus	9	11,903
Phaseolus vulgaris genome luana	08-16-2016 11:41 AM by luana	2	5,420

Page 1 of 10

Last »

Forum Tools	Search this Forum
Mark This Forum Read View Parent Forum	Search this Forum : Advanced Search

	New posts		Hot thread with new posts
	No new posts		Hot thread with no new posts
	Thread is closed

Posting Rules
You may not post new threads You may not post replies You may not post attachments You may not edit your posts BB code is On Smilies are On [IMG] code is On HTML code is Off Forum Rules

All times are GMT -8. The time now is 05:24 AM.