Genomic Resequencing

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Genomic Resequencing

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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	1,697
Find SNPs in related strains dsybers	10-09-2019 09:45 AM by dsybers	0	9,280
How to estimate genetic variation in a population with RNASeq data? dacotahm	09-26-2019 09:01 AM by dacotahm	0	2,669
Problem in mpileup file where size of sequence does not match size of quality cryptodice	08-04-2019 08:16 PM by cryptodice	0	3,615
Reliability of short insert sizes lburmz	05-14-2019 01:57 AM by lburmz	0	3,841
Variant and Genotype calling Alex_Dor	04-12-2019 06:22 AM by Alex_Dor	0	3,595
SNP calling on samples sequenced with different technology weehzer	09-10-2018 04:49 AM by weehzer	0	6,960
Calculate probability of a given sequence _anli	08-23-2018 09:24 AM by _anli	0	4,396
PL high support for each GT for all SNPS htetre	08-20-2018 12:05 PM by htetre	2	4,621
Experiences with SeqCap EZ Prime j_he	08-16-2018 04:29 PM by j_he	0	4,242
Adding GT tag to Strelka Output erichpeterson	08-09-2018 09:33 AM by GobiJerboa	1	6,762
The R-square between coverage and short variants number Chen-Tau Lin	07-31-2018 08:59 PM by Chen-Tau Lin	0	4,122
Control sample for human germline SNP discovery? whe	07-15-2018 07:11 PM by whe	0	4,644
SureSelect XT Probes icahn_seq	02-04-2018 09:28 AM by icahn_seq	2	6,739
SNPs at Interval Boundaries in GATK HaplotypeCaller peterlchang	10-24-2017 02:53 PM by peterlchang	0	6,113
Chromosomal translocation, which NGS method appropriate deepbiomed	09-13-2017 07:09 AM by r.rosati	4	6,956
mpileup only calling snps for chr1 not entire genome htetre	06-20-2017 02:56 PM by htetre	1	5,213
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	5,128
Calling variants when mapping reads from different species than reference gruberjd	05-19-2017 12:52 PM by Brian Bushnell	3	6,647
Panel Validation using NA12878 DNA NielQC	05-05-2017 04:36 AM by NielQC	0	5,777
How to generate VCF from HISAT2 pre-built SNP index? jol.espinoz	04-30-2017 12:03 PM by jol.espinoz	0	6,671
Somatic Mutation Amount cindylanzao	04-23-2017 06:02 PM by cindylanzao	0	5,240
Coverage of reads not homogenous (sureselect target enrichement) Sam64	04-14-2017 09:37 AM by czhang	2	7,186
Removing duplicate PacBio reads AgatheJ	02-19-2017 09:38 AM by AgatheJ	8	7,886
CONTRA cnv on chrX Michel Meyer	02-06-2017 09:00 AM by Michel Meyer	0	5,162
hope to know the softwares to plot this image about genomic linkage map zhdorothy	12-12-2016 07:22 PM by zhdorothy	0	6,106
fastq.gz size for human WGS coverage calculation yipukangda	11-08-2016 06:26 PM by yipukangda	2	6,937
Abnormaly amount of reads Mr.Zurich1992	10-02-2016 03:44 AM by dpryan	1	5,826
Illumina vs. Agilent Exome enrichment - higher false positive rates markusl	09-22-2016 08:22 AM by Geneus	9	12,236
Phaseolus vulgaris genome luana	08-16-2016 11:41 AM by luana	2	5,686

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