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Comment: C: add sample name to bam header based on bam file name
3.9 years ago by Ana ▴ 200
1
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1
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6.5k
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Comment: C: add sample name to bam header based on bam file name
3.9 years ago by Ana ▴ 200
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0
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6.1k
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Comment: C: VariantsToTable in GATK does not produce the table of all SNPs in the vcf file
6.3 years ago by Ana ▴ 200
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1
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4.7k
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Comment: C: compute correlation for depth of coverage between 2 datasets with different leng
6.6 years ago by Ana ▴ 200
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1
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4.7k
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Comment: C: compute correlation for depth of coverage between 2 datasets with different leng
6.6 years ago by Ana ▴ 200
0
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1
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4.7k
views
Comment: C: compute correlation for depth of coverage between 2 datasets with different leng
6.6 years ago by Ana ▴ 200
0
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1
reply
4.7k
views
Comment: C: compute correlation for depth of coverage between 2 datasets with different leng
6.6 years ago by Ana ▴ 200
0
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1
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4.7k
views
Comment: C: compute correlation for depth of coverage between 2 datasets with different leng
6.6 years ago by Ana ▴ 200
0
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1
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1.6k
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Comment: C: attaching genotypes in the vcf files to individual ID
6.6 years ago by Ana ▴ 200
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1
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1.6k
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Comment: C: attaching genotypes in the vcf files to individual ID
6.6 years ago by Ana ▴ 200
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0
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2.6k
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Comment: C: no output after running samtools depth
6.6 years ago by Ana ▴ 200
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1
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2.6k
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Comment: C: no output after running samtools depth
6.6 years ago by Ana ▴ 200
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3
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6.5k
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Comment: C: compute depth of coverage for certain regions of the genome using samtools depth
6.6 years ago by Ana ▴ 200
0
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1
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6.5k
views
Comment: C: compute depth of coverage for certain regions of the genome using samtools depth
6.6 years ago by Ana ▴ 200
0
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2
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6.5k
views
Comment: C: compute depth of coverage for certain regions of the genome using samtools depth
6.6 years ago by Ana ▴ 200
0
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1
reply
6.5k
views
Comment: C: compute depth of coverage for certain regions of the genome using samtools depth
6.6 years ago by Ana ▴ 200
0
votes
1
reply
6.5k
views
Comment: C: compute depth of coverage for certain regions of the genome using samtools depth
6.6 years ago by Ana ▴ 200
0
votes
1
reply
6.5k
views
Comment: C: compute depth of coverage for certain regions of the genome using samtools depth
6.6 years ago by Ana ▴ 200
0
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1
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4.7k
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Comment: C: downloading bam files of phase 3 of 1000 genomes project
6.6 years ago by Ana ▴ 200
0
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1
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4.7k
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Comment: C: downloading bam files of phase 3 of 1000 genomes project
6.6 years ago by Ana ▴ 200
0
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1
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4.7k
views
Comment: C: downloading bam files of phase 3 of 1000 genomes project
6.6 years ago by Ana ▴ 200
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1
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2.0k
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Comment: C: multiple DNA reads aligned to the same gene
6.9 years ago by Ana ▴ 200
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1
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2.0k
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Comment: C: multiple DNA sequences aligned to the same gene
6.9 years ago by Ana ▴ 200
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0
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1.5k
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Comment: C: Software to analyze Diamond data
6.9 years ago by Ana ▴ 200
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1
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1.8k
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Comment: C: finding candidate genes and their annotations
6.9 years ago by Ana ▴ 200
1
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0
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2.5k
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Comment: C: how to adjust a Manhattan plot for bayes factor
7.1 years ago by Ana ▴ 200
1
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1
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2.5k
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Comment: C: convert population allele count data into population allele frequency
7.2 years ago by Ana ▴ 200
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1
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2.5k
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Comment: C: convert population allele count data into population allele frequency
7.2 years ago by Ana ▴ 200
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1
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2.5k
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Comment: C: convert population allele count data into population allele frequency
7.2 years ago by Ana ▴ 200
0
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0
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1.6k
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Comment: C: conditional replacing rows with 9
7.2 years ago by Ana ▴ 200
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0
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1.6k
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Comment: C: conditional replacing rows with 9
7.2 years ago by Ana ▴ 200
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2
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1.6k
views
Comment: C: conditional replacing rows with 9
7.2 years ago by Ana ▴ 200
1
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0
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1.5k
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Comment: C: how to calculate the proportion of SNPs with DP more than 5
7.2 years ago by Ana ▴ 200
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1
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1.9k
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Comment: C: how to extract DP for individuals from the same population and save them in a fi
7.2 years ago by Ana ▴ 200
0
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1
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5.4k
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Comment: C: 012 genotype matrix using vcf tools (converting rows to columns)
7.2 years ago by Ana ▴ 200
0
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1
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5.4k
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Comment: C: 012 genotype matrix using vcf tools (converting rows to columns)
7.2 years ago by Ana ▴ 200
0
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0
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15k
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Comment: C: SnpMatrix from VCF file
7.2 years ago by Ana ▴ 200
0
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1
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5.4k
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Comment: C: 012 genotype matrix using vcf tools (converting rows to columns)
7.2 years ago by Ana ▴ 200
0
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1
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2.5k
views
Comment: C: error with running distruct.py in fastSTRUCTURE
7.3 years ago by Ana ▴ 200
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1
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5.1k
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Comment: C: running a perl script multiple times; input and output files are required
7.4 years ago by Ana ▴ 200
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0
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5.1k
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Comment: C: running a perl script multiple times; input and output files are required
7.4 years ago by Ana ▴ 200
1
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0
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1.4k
views
Comment: C: extract groups of SnPs and store them in separate files
7.4 years ago by Ana ▴ 200
0
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0
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1.9k
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Comment: C: how can I keep only those SNP in file "a" which match to SNPs in file "b"?
7.4 years ago by Ana ▴ 200
0
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1
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3.5k
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Comment: C: restructure rows and columns in perl or python (Interleaving columns by row pair
7.5 years ago by Ana ▴ 200
0
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1
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3.5k
views
Comment: C: how to extract a random set of SNP from a SNP table
7.6 years ago by Ana ▴ 200
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1
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3.5k
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Comment: C: how to extract a random set of SNP from a SNP table
7.6 years ago by Ana ▴ 200
0
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1
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3.5k
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Comment: C: how to extract a random set of SNP from a SNP table
7.6 years ago by Ana ▴ 200
0
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1
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3.5k
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Comment: C: how to extract a random set of SNP from a SNP table
7.6 years ago by Ana ▴ 200
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2
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4.0k
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Comment: A: extract sample DP values from VCF
7.7 years ago by Ana ▴ 200
0
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0
replies
3.2k
views
Comment: C: calculating genotype quality from genotype likelihood
7.7 years ago by Ana ▴ 200
51 results • Page 1 of 2
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