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questions
1
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2
replies
472
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A question about the missing or not observed alleles in PLINK datasets
PLINK
5 months ago by
abedkurdi10
▴ 190
1
vote
6
replies
921
views
A question about genotyping rate
genotyping
snps
harmonizer
array
6 months ago by
abedkurdi10
▴ 190
4
votes
4
replies
755
views
DESeq2 analysis using two featureCounts generated from different studies
RNA-seq
DESeq2
7 months ago by
abedkurdi10
▴ 190
0
votes
0
replies
424
views
A question about GWENA R/Bioconductor package
proteomics
wgcna
gwena
17 months ago by
abedkurdi10
▴ 190
0
votes
4
replies
955
views
RNA-seq Infer experiment wrong strandeness information
RNA-Seq
rseqc
infer_experiment
3.8 years ago by
abedkurdi10
▴ 190
0
votes
2
replies
1.2k
views
Bigwig circular plot
bigwig
javascript
java
updated 10 months ago by
Ram
43k • written 4.1 years ago by
abedkurdi10
▴ 190
4
votes
10
replies
2.3k
views
Optimal number of samples needed to detect a variant from panel sequencing
exome
sequencing
variants
samples
7.2 years ago by
abedkurdi10
▴ 190
3
votes
1
reply
1.5k
views
Error in Rscript
R
error
Rscript
updated 7.2 years ago by
Alex Reynolds
35k • written 7.2 years ago by
abedkurdi10
▴ 190
2
votes
2
replies
2.2k
views
Statistics on BED files
bed
statistics
intervals
updated 7.3 years ago by
Alex Reynolds
35k • written 7.3 years ago by
abedkurdi10
▴ 190
5
votes
6
replies
3.9k
views
Thresholds to filter out variants from vcf file
vcf
thresholds
filtering
updated 7.5 years ago by
Ron
★ 1.2k • written 7.5 years ago by
abedkurdi10
▴ 190
2
votes
4
replies
4.6k
views
VCF file re-header
vcf header
vcf
reheader
7.5 years ago by
abedkurdi10
▴ 190
0
votes
6
replies
4.4k
views
Clinical significance explanation
clinvar
clinical significance
updated 7.5 years ago by
Devon Ryan
104k • written 7.5 years ago by
abedkurdi10
▴ 190
0
votes
1
reply
4.6k
views
raw data (fastq files) of whole exome sequencing (WES) of somatic mutations
somatic
wes
samples
updated 7.7 years ago by
Medhat
9.7k • written 7.7 years ago by
abedkurdi10
▴ 190
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