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1
reply
1.9k
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Comment:
C: De-replicating sequence file after barcodes/primers removed.
6.3 years ago by
pfs
▴ 280
0
votes
2
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2.0k
views
Answer:
A: Multiple testing correction in linear mixed models (MLM) for GWAS
6.3 years ago by
pfs
▴ 280
1
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1
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1.3k
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Answer:
A: Where can I find the info about the start/end position of sets of SNP's that are
6.8 years ago by
pfs
▴ 280
1
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0
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1.7k
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Comment:
C: how to combain microarray sets from the same platform but raw data were normaliz
6.8 years ago by
pfs
▴ 280
1
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1
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1.7k
views
Answer:
A: how to combain microarray sets from the same platform but raw data were normaliz
6.8 years ago by
pfs
▴ 280
0
votes
0
replies
2.1k
views
Answer:
A: Regenotype vcf using some samples as reference
6.8 years ago by
pfs
▴ 280
0
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0
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1.7k
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Answer:
A: finding function of genes from their coordinates
6.9 years ago by
pfs
▴ 280
0
votes
0
replies
1.5k
views
Comment:
C: Samtools mpileup ends abruptly without completing full analysis
6.9 years ago by
pfs
▴ 280
0
votes
0
replies
1.4k
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Comment:
C: Given QTLs and genome annotation, quickly list genes closest to QTLs
6.9 years ago by
pfs
▴ 280
0
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1
reply
2.1k
views
Comment:
C: how to annotate chromosome position with the gene list file
6.9 years ago by
pfs
▴ 280
3
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1
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3.9k
views
Answer:
A: Suggestions regarding bioinformatics journal
6.9 years ago by
pfs
▴ 280
0
votes
1
reply
1.5k
views
Answer:
A: SNPSVM - not able to find VCF file
6.9 years ago by
pfs
▴ 280
0
votes
1
reply
1.4k
views
Answer:
A: Given QTLs and genome annotation, quickly list genes closest to QTLs
7.0 years ago by
pfs
▴ 280
0
votes
1
reply
1.5k
views
Answer:
A: SNPSVM - not able to find VCF file
7.0 years ago by
pfs
▴ 280
4
votes
1
reply
2.4k
views
Answer:
A: SNP calling from a scaffold.fa file
7.0 years ago by
pfs
▴ 280
0
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2
replies
4.9k
views
Answer:
A: value too large for defined data type using bgzip
7.0 years ago by
pfs
▴ 280
0
votes
1
reply
7.3k
views
Comment:
C: Stuck on calculating principal components
7.0 years ago by
pfs
▴ 280
0
votes
2
replies
7.3k
views
Comment:
C: Stuck on calculating principal components
7.0 years ago by
pfs
▴ 280
5
votes
0
replies
1.7k
views
Answer:
A: (Sanity check) Too many SNPs?
7.1 years ago by
pfs
▴ 280
1
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0
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1.5k
views
Answer:
A: Finding GO terms for an organism not in a GO database
7.1 years ago by
pfs
▴ 280
1
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0
replies
1.8k
views
Answer:
A: Conditional analysis on dosage file -what program to use?
7.1 years ago by
pfs
▴ 280
1
vote
1
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7.0k
views
Answer:
A: How to make variant calling run faster?
7.1 years ago by
pfs
▴ 280
0
votes
0
replies
6.1k
views
Answer:
A: Compare between two columns of two different files and print common
7.1 years ago by
pfs
▴ 280
0
votes
1
reply
6.1k
views
Answer:
A: Compare between two columns of two different files and print common
7.1 years ago by
pfs
▴ 280
2
votes
0
replies
1.3k
views
Answer:
A: difference between 2 snp's data annotations
7.1 years ago by
pfs
▴ 280
3
votes
0
replies
5.3k
views
Answer:
A: How to find the unique list of mismatches of reads with the reference genome
7.1 years ago by
pfs
▴ 280
1
vote
0
replies
3.3k
views
Answer:
A: Reference and mutant allele of a SNP rsID
7.1 years ago by
pfs
▴ 280
0
votes
0
replies
1.6k
views
Comment:
C: Indentical proteins but different Blast results
7.2 years ago by
pfs
▴ 280
0
votes
1
reply
1.6k
views
Answer:
A: Indentical proteins but different Blast results
7.2 years ago by
pfs
▴ 280
0
votes
0
replies
3.7k
views
Answer:
A: Subsetting individuals in PLINK when IDs contain underscores "_"
7.2 years ago by
pfs
▴ 280
0
votes
0
replies
6.2k
views
Comment:
C: Using Plink, get allele frequencies for a subset of individuals
7.2 years ago by
pfs
▴ 280
0
votes
1
reply
6.2k
views
Answer:
A: Using Plink, get allele frequencies for a subset of individuals
7.2 years ago by
pfs
▴ 280
1
vote
1
reply
10k
views
Answer:
A: plink calculating LD using R2 command
7.2 years ago by
pfs
▴ 280
0
votes
1
reply
1.9k
views
Answer:
A: Recode SNPs dataset to Number
7.2 years ago by
pfs
▴ 280
1
vote
0
replies
2.2k
views
Answer:
A: VCF mining & interpretation tools (hg38 build)
7.2 years ago by
pfs
▴ 280
1
vote
1
reply
2.2k
views
Answer:
A: VCF mining & interpretation tools (hg38 build)
7.2 years ago by
pfs
▴ 280
0
votes
0
replies
3.0k
views
Comment:
C: How to remove reads in a fastq file that DO NOT have adapter sequence in them?
7.3 years ago by
pfs
▴ 280
0
votes
0
replies
1.6k
views
Comment:
C: Any kind of sequences are AT-rich on the human genome
7.3 years ago by
pfs
▴ 280
0
votes
2
replies
1.6k
views
Comment:
A: Normalization for NGS count data with high variance between observations / uneve
7.3 years ago by
pfs
▴ 280
0
votes
1
reply
3.0k
views
Comment:
C: HaplotypeCaller filter out variants covered only in one direction
7.3 years ago by
pfs
▴ 280
0
votes
1
reply
3.0k
views
Answer:
A: HaplotypeCaller filter out variants covered only in one direction
7.3 years ago by
pfs
▴ 280
0
votes
0
replies
2.8k
views
Answer:
A: Any great tutorials on how to download sift/provean on your computer?
7.3 years ago by
pfs
▴ 280
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