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3.3k
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Comment:
C: Extract bed regions from CRAM files
4.2 years ago by
MAPK
★ 2.1k
3
votes
8
replies
3.3k
views
Extract bed regions from CRAM files
BAM
CRAM
4.2 years ago by
MAPK
★ 2.1k
0
votes
1
reply
1.1k
views
SRA to paired fastq per read group
sra
NGS
updated 4.2 years ago by
GenoMax
148k • written 4.3 years ago by
MAPK
★ 2.1k
0
votes
0
replies
2.3k
views
Comment:
C: How to create custom docker image to download bam files from SRA
4.3 years ago by
MAPK
★ 2.1k
6
votes
4
replies
2.3k
views
How to create custom docker image to download bam files from SRA
docker
updated 17 months ago by
1769mkc
★ 1.2k • written 4.3 years ago by
MAPK
★ 2.1k
0
votes
1
reply
3.8k
views
Comment:
C: Plink --merge-list generating error
4.3 years ago by
MAPK
★ 2.1k
3
votes
3
replies
3.8k
views
Plink --merge-list generating error
plink
updated 4.3 years ago by
Sam
★ 4.8k • written 4.3 years ago by
MAPK
★ 2.1k
0
votes
3
replies
1.4k
views
How to calculate maf for a variant for case and control
MAF
genetics
variant
4.3 years ago by
MAPK
★ 2.1k
0
votes
0
replies
1.4k
views
Comment:
C: How to calculate maf for a variant for case and control
4.3 years ago by
MAPK
★ 2.1k
0
votes
0
replies
1.2k
views
Comment:
C: Dealing with GATK illegal character
4.3 years ago by
MAPK
★ 2.1k
2
votes
2
replies
1.2k
views
Dealing with GATK illegal character
gatk
4.3 years ago by
MAPK
★ 2.1k
4
votes
5
replies
1.5k
views
How to set sleep in GNU parallel in a esearch/efetch script
sra
ncbi
programming
shell
updated 4.4 years ago by
ole.tange
★ 4.5k • written 4.4 years ago by
MAPK
★ 2.1k
0
votes
1
reply
1.5k
views
Comment:
C: How to set sleep in GNU parallel in a esearch/efetch script
4.4 years ago by
MAPK
★ 2.1k
0
votes
2
replies
1.1k
views
Understanding filters used in plink
plink
updated 4.4 years ago by
h.mon
35k • written 4.4 years ago by
MAPK
★ 2.1k
3
votes
10
replies
4.1k
views
8 follow
Phylogenetic analysis for large size fasta sequences
phylogenetics
updated 3.6 years ago by
Shri hari
▴ 40 • written 6.5 years ago by
MAPK
★ 2.1k
2
votes
2
replies
1.9k
views
GATK version differences
GATK
4.4 years ago by
MAPK
★ 2.1k
1
vote
1
reply
3.6k
views
Converting Variant ID to RsID in batch
SNP
rsID
4.4 years ago by
MAPK
★ 2.1k
3
votes
1
reply
1.5k
views
VEP output and protein change
VEP
VCF
updated 4.4 years ago by
Ram
44k • written 4.4 years ago by
MAPK
★ 2.1k
2
votes
1
reply
1.3k
views
How to combining VEP and VCF in one file
vcf
vep
updated 4.4 years ago by
Pierre Lindenbaum
164k • written 4.4 years ago by
MAPK
★ 2.1k
2
votes
3
replies
1.1k
views
Intersect exome region from whole genome gvcf
gatk
GenomicsDBImport
4.5 years ago by
MAPK
★ 2.1k
0
votes
1
reply
1.1k
views
Comment:
C: Intersect exome region from whole genome gvcf
4.5 years ago by
MAPK
★ 2.1k
0
votes
0
replies
3.8k
views
Comment:
C: GATK GenomicsDBImport intervals
4.5 years ago by
MAPK
★ 2.1k
1
vote
2
replies
3.8k
views
GATK GenomicsDBImport intervals
GATK
gvcf
4.5 years ago by
MAPK
★ 2.1k
0
votes
0
replies
506
views
Mismatch table from pariwise sequence alignment
alignment
4.6 years ago by
MAPK
★ 2.1k
9
votes
3
replies
1.3k
views
How to cite datasets downloaded from Ensembl?
Citation
Ensembl
updated 4.8 years ago by
Astrid_Ensembl
▴ 330 • written 4.8 years ago by
MAPK
★ 2.1k
0
votes
2
replies
1.4k
views
Cross assembly of metagenomics
RNA-Seq
updated 4.8 years ago by
onestop_data
▴ 330 • written 5.8 years ago by
MAPK
★ 2.1k
4
votes
6
replies
7.5k
views
How to extract chrX, chrY and chrM from a vcf file?
VCF
updated 4.8 years ago by
yiqiangz
▴ 10 • written 8.3 years ago by
MAPK
★ 2.1k
0
votes
0
replies
1.3k
views
Comment:
C: GFF file for soybean RNAseq analysis
4.8 years ago by
MAPK
★ 2.1k
2
votes
2
replies
1.3k
views
GFF file for soybean RNAseq analysis
RNA-Seq
updated 4.8 years ago by
Brice Sarver
★ 3.8k • written 4.8 years ago by
MAPK
★ 2.1k
8
votes
9
replies
9.8k
views
Translate Dna To Protein Using Transeq
dna
updated 4.9 years ago by
Biostar
20 • written 10.7 years ago by
MAPK
★ 2.1k
0
votes
0
replies
2.2k
views
Comment:
C: Why is it important to control ethnicity when studying rare variants?
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
MAPK
★ 2.1k
1
vote
0
replies
13k
views
Answer:
A: how to get the genotypes from vcf file.
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
MAPK
★ 2.1k
0
votes
1
reply
2.2k
views
Comment:
C: Why is it important to control ethnicity when studying rare variants?
updated 4.9 years ago by
Ram
44k • written 8.8 years ago by
MAPK
★ 2.1k
0
votes
1
reply
2.3k
views
Comment:
C: How to find the variant type, location and effects (synonymous/nonsynonymous)
updated 4.9 years ago by
Ram
44k • written 8.9 years ago by
MAPK
★ 2.1k
4
votes
3
replies
1.2k
views
How to decide on a reasonable title for a bioinformatics talk
interview
career
updated 21 months ago by
Ram
44k • written 4.9 years ago by
MAPK
★ 2.1k
0
votes
0
replies
1.2k
views
Comment:
C: How to decide on a reasonable title for a bioinformatics talk
4.9 years ago by
MAPK
★ 2.1k
0
votes
0
replies
5.8k
views
Comment:
C: IBD vs IBS
updated 5.0 years ago by
Ram
44k • written 8.9 years ago by
MAPK
★ 2.1k
0
votes
1
reply
2.7k
views
Comment:
C: Statistical analysis to compare three different variables
updated 5.0 years ago by
Ram
44k • written 8.9 years ago by
MAPK
★ 2.1k
1
vote
1
reply
2.8k
views
Comment:
C: What could be the reason for having mutations in too many cancer samples?
updated 5.0 years ago by
Ram
44k • written 8.9 years ago by
MAPK
★ 2.1k
0
votes
2
replies
2.8k
views
Comment:
C: What could be the reason for having mutations in too many cancer samples?
updated 5.0 years ago by
Ram
44k • written 8.9 years ago by
MAPK
★ 2.1k
0
votes
1
reply
2.8k
views
Comment:
C: What could be the reason for having mutations in too many cancer samples?
updated 5.0 years ago by
Ram
44k • written 8.9 years ago by
MAPK
★ 2.1k
0
votes
1
reply
15k
views
Comment:
C: What is GFF3 and how to extract genomic sequences from it?
updated 5.0 years ago by
Ram
44k • written 10.6 years ago by
MAPK
★ 2.1k
0
votes
0
replies
15k
views
Comment:
C: What is GFF3 and how to extract genomic sequences from it?
updated 5.0 years ago by
Ram
44k • written 10.6 years ago by
MAPK
★ 2.1k
0
votes
1
reply
44k
views
Comment:
C: How To Get Bed File Containing Exons Of Canonical Transcripts And Their Correspo
updated 5.0 years ago by
Ram
44k • written 8.9 years ago by
MAPK
★ 2.1k
0
votes
0
replies
6.2k
views
Comment:
C: Mastervar - Complete Genomics Data Format To Vcf
updated 5.0 years ago by
Ram
44k • written 9.0 years ago by
MAPK
★ 2.1k
0
votes
0
replies
11k
views
Comment:
C: What are the terms for reference allele and alternate alleles in cancer?
updated 5.0 years ago by
Ram
44k • written 9.1 years ago by
MAPK
★ 2.1k
1
vote
0
replies
3.7k
views
Comment:
C: How Many Cells Will Be Involved In One Dna Or Rna Sequencing?
updated 5.0 years ago by
Ram
44k • written 9.1 years ago by
MAPK
★ 2.1k
0
votes
0
replies
4.5k
views
Comment:
C: Get multiple snps coverage (allelic depth) from bam files
updated 5.0 years ago by
Ram
44k • written 9.1 years ago by
MAPK
★ 2.1k
0
votes
1
reply
4.5k
views
Comment:
C: Get multiple snps coverage (allelic depth) from bam files
updated 5.0 years ago by
Ram
44k • written 9.1 years ago by
MAPK
★ 2.1k
0
votes
1
reply
4.0k
views
Comment:
C: IBD calculation with Plink
5.0 years ago by
MAPK
★ 2.1k
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