Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
0
votes
0
replies
3.4k
views
Comment: C: How To Import Tsv-File In Gene Ontology Or Annotate-It?
6.4 years ago by vivekruhela ▴ 20
0
votes
0
replies
2.8k
views
Comment: C: Simple count of dbSNP (rs...) from .vcf file
6.6 years ago by vivekruhela ▴ 20
0
votes
0
replies
3.1k
views
Comment: C: filtering pindel results
6.6 years ago by vivekruhela ▴ 20
0
votes
0
replies
1.0k
views
Information about control data
genome next-gen sequencing sequence
6.6 years ago by vivekruhela ▴ 20
0
votes
0
replies
3.9k
views
Comment: C: How to combine multiple tools to detct SVs in WES data
6.6 years ago by vivekruhela ▴ 20
0
votes
1
reply
2.0k
views
Comment: C: How to determine high-quality somatic mutations
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
1.3k
views
How to get unique somatic mutations for each individual patients
next-gen R snp sequence gene
6.7 years ago by vivekruhela ▴ 20
0
votes
1
reply
16k
views
Comment: C: Obtaining uniquely mapped reads from BWA mem alignment (filtering by q score doe
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
2.7k
views
Comment: C: Percentage of uniquely mapped reads
6.7 years ago by vivekruhela ▴ 20
0
votes
2
replies
23k
views
Comment: C: should I merge fastq files for different lanes before do QC?
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
28k
views
Comment: C: Converting Gvcf Files Into Vcf
6.7 years ago by vivekruhela ▴ 20
0
votes
1
reply
28k
views
Comment: C: Converting Gvcf Files Into Vcf
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
2.7k
views
Comment: C: Percentage of uniquely mapped reads
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
6.1k
views
Comment: C: Truncated Bam Error
6.7 years ago by vivekruhela ▴ 20
1
vote
2
replies
6.1k
views
Answer: A: Truncated Bam Error
6.7 years ago by vivekruhela ▴ 20
1
vote
11
replies
6.1k
views
Truncated Bam Error
R next-gen sequencing software error
updated 6 months ago by • 0 • written 6.7 years ago by ▴ 20
2
votes
4
replies
2.7k
views
Percentage of uniquely mapped reads
R sequencing next-gen alignment
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
6.1k
views
Comment: C: Truncated Bam Error
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
6.1k
views
Comment: C: Truncated Bam Error
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
6.1k
views
Comment: C: Truncated Bam Error
6.7 years ago by vivekruhela ▴ 20
0
votes
1
reply
6.1k
views
Comment: C: Truncated Bam Error
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
3.9k
views
Comment: C: How to combine multiple tools to detct SVs in WES data
6.7 years ago by vivekruhela ▴ 20
0
votes
2
replies
3.9k
views
Comment: C: How to combine multiple tools to detct SVs in WES data
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
2.0k
views
Comment: C: How to determine high-quality somatic mutations
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
2.0k
views
Comment: C: How to determine high-quality somatic mutations
6.7 years ago by vivekruhela ▴ 20
0
votes
2
replies
2.0k
views
Comment: C: How to determine high-quality somatic mutations
6.7 years ago by vivekruhela ▴ 20
0
votes
8
replies
2.0k
views
How to determine high-quality somatic mutations
R next-gen sequence somatic-mutations
6.7 years ago by vivekruhela ▴ 20
0
votes
1
reply
4.6k
views
Comment: C: How to deal with Unplace Chromosome (chrUn)
6.7 years ago by vivekruhela ▴ 20
2
votes
3
replies
4.6k
views
How to deal with Unplace Chromosome (chrUn)
R next-gen genome SNP
updated 6.7 years ago by 8.7k • written 6.7 years ago by ▴ 20
1
vote
0
replies
2.9k
views
Comment: C: Difference between gene-based, region-based and filter-based annotation in ANNOV
6.7 years ago by vivekruhela ▴ 20
4
votes
2
replies
2.9k
views
Difference between gene-based, region-based and filter-based annotation in ANNOVAR
next-gen R sequence gene annotation
updated 6.7 years ago by 88k • written 6.7 years ago by ▴ 20
0
votes
1
reply
3.9k
views
Answer: A: How to combine multiple tools to detct SVs in WES data
6.7 years ago by vivekruhela ▴ 20
7
votes
14
replies
3.9k
views
How to combine multiple tools to detct SVs in WES data
SNP R next-gen sequence snp
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
3.5k
views
Comment: C: Error : Duplicate allele added to VariantContext GATK
6.7 years ago by vivekruhela ▴ 20
0
votes
1
reply
3.9k
views
Comment: C: How to combine multiple tools to detct SVs in WES data
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
3.9k
views
Comment: C: How to combine multiple tools to detct SVs in WES data
6.7 years ago by vivekruhela ▴ 20
0
votes
0
replies
1.4k
views
Comment: C: Get fastq files back from LRPatterns output
6.8 years ago by vivekruhela ▴ 20
0
votes
0
replies
1.4k
views
Comment: C: Get fastq files back from LRPatterns output
6.8 years ago by vivekruhela ▴ 20
0
votes
3
replies
1.4k
views
Get fastq files back from LRPatterns output
R trimmer adaptor sequencing
6.8 years ago by vivekruhela ▴ 20
39 results • Page 1 of 1
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6