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933
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Comment:
C: Removing GC dinucleotides from a sequence
4.1 years ago by
spiral01
▴ 110
0
votes
1
reply
1.9k
views
Comment:
C: Bioawk - using bash variables
4.8 years ago by
spiral01
▴ 110
0
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0
replies
1.6k
views
Comment:
C: 1000 genomes coding SNPs not in exonic regions?
5.3 years ago by
spiral01
▴ 110
0
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1
reply
1.6k
views
Comment:
C: 1000 genomes coding SNPs not in exonic regions?
5.3 years ago by
spiral01
▴ 110
0
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1
reply
1.6k
views
Comment:
C: 1000 genomes coding SNPs not in exonic regions?
5.3 years ago by
spiral01
▴ 110
0
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0
replies
1.6k
views
Comment:
C: 1000 genomes coding SNPs not in exonic regions?
5.3 years ago by
spiral01
▴ 110
0
votes
1
reply
1.6k
views
Comment:
C: 1000 genomes coding SNPs not in exonic regions?
5.3 years ago by
spiral01
▴ 110
0
votes
0
replies
3.4k
views
Comment:
C: Set ancestral alleles to upper case in vcf file
6.1 years ago by
spiral01
▴ 110
0
votes
0
replies
13k
views
Comment:
C: Writing vcf file headers
6.2 years ago by
spiral01
▴ 110
0
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1
reply
13k
views
Comment:
C: Writing vcf file headers
6.2 years ago by
spiral01
▴ 110
0
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0
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13k
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Comment:
C: Writing vcf file headers
6.2 years ago by
spiral01
▴ 110
0
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1
reply
13k
views
Comment:
C: Writing vcf file headers
6.2 years ago by
spiral01
▴ 110
0
votes
1
reply
13k
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Comment:
C: Writing vcf file headers
6.2 years ago by
spiral01
▴ 110
1
vote
0
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2.5k
views
Comment:
C: counting number of variants within specified windows
6.3 years ago by
spiral01
▴ 110
0
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0
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2.5k
views
Comment:
C: counting number of variants within specified windows
6.3 years ago by
spiral01
▴ 110
0
votes
0
replies
5.9k
views
Comment:
C: bedtools window - killed: 9 error
6.4 years ago by
spiral01
▴ 110
0
votes
1
reply
5.9k
views
Comment:
C: bedtools window - killed: 9 error
6.4 years ago by
spiral01
▴ 110
0
votes
1
reply
5.9k
views
Comment:
C: bedtools window - killed: 9 error
6.4 years ago by
spiral01
▴ 110
0
votes
1
reply
5.9k
views
Comment:
C: bedtools window - killed: 9 error
6.4 years ago by
spiral01
▴ 110
0
votes
1
reply
4.5k
views
Comment:
C: vcf files: counting number of variants in genomic windows of chosen size
6.4 years ago by
spiral01
▴ 110
0
votes
0
replies
16k
views
Comment:
C: Plotting SNP density along a chromosome from VCF files
6.4 years ago by
spiral01
▴ 110
0
votes
0
replies
4.5k
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Comment:
C: vcf files: counting number of variants in genomic windows of chosen size
6.4 years ago by
spiral01
▴ 110
0
votes
1
reply
2.3k
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Comment:
C: Combining vcf files so that same loci data is combined
6.4 years ago by
spiral01
▴ 110
0
votes
1
reply
2.3k
views
Comment:
C: Combining vcf files so that same loci data is combined
6.4 years ago by
spiral01
▴ 110
0
votes
1
reply
1.6k
views
Comment:
C: Precedence between alt field and GT info in vcf files
6.4 years ago by
spiral01
▴ 110
0
votes
0
replies
5.8k
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Comment:
C: Quickest way to filter vcf using bed files
6.4 years ago by
spiral01
▴ 110
0
votes
0
replies
5.8k
views
Comment:
C: Quickest way to filter vcf using bed files
6.4 years ago by
spiral01
▴ 110
0
votes
1
reply
5.8k
views
Comment:
C: Quickest way to filter vcf using bed files
6.4 years ago by
spiral01
▴ 110
0
votes
0
replies
1.4k
views
Comment:
C: Annotating Altai Neanderthal and Denisovan variants
6.5 years ago by
spiral01
▴ 110
0
votes
1
reply
2.0k
views
Comment:
C: Discrepencies between ANNOVAR and Gencode annotations of 1000 genomes
6.6 years ago by
spiral01
▴ 110
0
votes
1
reply
2.0k
views
Comment:
C: Discrepencies between ANNOVAR and Gencode annotations of 1000 genomes
6.6 years ago by
spiral01
▴ 110
0
votes
1
reply
2.0k
views
Comment:
C: Discrepencies between ANNOVAR and Gencode annotations of 1000 genomes
6.6 years ago by
spiral01
▴ 110
0
votes
1
reply
2.0k
views
Comment:
C: Discrepencies between ANNOVAR and Gencode annotations of 1000 genomes
6.6 years ago by
spiral01
▴ 110
0
votes
1
reply
2.0k
views
Comment:
C: Discrepencies between ANNOVAR and Gencode annotations of 1000 genomes
6.6 years ago by
spiral01
▴ 110
0
votes
1
reply
3.1k
views
Comment:
C: Using multiple filters in BiomaRt's getSequence
6.7 years ago by
spiral01
▴ 110
0
votes
1
reply
1.8k
views
Comment:
C: Denisovan and Altai Neanderthal .bed files?
6.7 years ago by
spiral01
▴ 110
0
votes
0
replies
1.3k
views
Comment:
C: Estimating site information from 1000 genomes vcf data
6.7 years ago by
spiral01
▴ 110
0
votes
1
reply
2.4k
views
Comment:
C: 1000genomes: choosing the best annotation from multiple transcripts
6.8 years ago by
spiral01
▴ 110
0
votes
1
reply
2.4k
views
Comment:
C: 1000genomes: choosing the best annotation from multiple transcripts
6.8 years ago by
spiral01
▴ 110
0
votes
0
replies
4.3k
views
Comment:
C: How large are 1000genomes vcf files?
6.8 years ago by
spiral01
▴ 110
1
vote
2
replies
4.3k
views
Comment:
C: How large are 1000genomes vcf files?
6.8 years ago by
spiral01
▴ 110
1
vote
0
replies
4.3k
views
Comment:
C: How large are 1000genomes vcf files?
6.8 years ago by
spiral01
▴ 110
1
vote
1
reply
4.3k
views
Comment:
C: How large are 1000genomes vcf files?
6.8 years ago by
spiral01
▴ 110
0
votes
1
reply
4.3k
views
Comment:
C: How large are 1000genomes vcf files?
6.8 years ago by
spiral01
▴ 110
0
votes
0
replies
2.3k
views
Comment:
C: Acquiring and combining hg38 SNP and gene data
6.9 years ago by
spiral01
▴ 110
0
votes
1
reply
2.3k
views
Comment:
C: Acquiring and combining hg38 SNP and gene data
6.9 years ago by
spiral01
▴ 110
0
votes
1
reply
2.3k
views
Comment:
C: Acquiring and combining hg38 SNP and gene data
6.9 years ago by
spiral01
▴ 110
0
votes
1
reply
2.3k
views
Comment:
C: Acquiring and combining hg38 SNP and gene data
6.9 years ago by
spiral01
▴ 110
0
votes
1
reply
2.3k
views
Comment:
C: Acquiring and combining hg38 SNP and gene data
6.9 years ago by
spiral01
▴ 110
0
votes
0
replies
2.3k
views
Comment:
C: Calculating LRT of a phylogenetic tree (as in codeml)
7.7 years ago by
spiral01
▴ 110
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