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Comment: C: Command to extract SNPs from VCF file using bcftool
9.6 years ago by Jorge Amigo 14k
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Comment: C: samtools mpeileup: extract SNPs between individuals only (discard SNPs betn indi
9.6 years ago by Jorge Amigo 14k
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Answer: A: Command to extract SNPs from VCF file using bcftool
9.6 years ago by Jorge Amigo 14k
0
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1
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3.1k
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Answer: A: samtools mpeileup: extract SNPs between individuals only (discard SNPs betn indi
9.6 years ago by Jorge Amigo 14k
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1.8k
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Comment: C: How to get the SNP statistics for Hg19
9.6 years ago by Jorge Amigo 14k
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Comment: C: Any tool to get SNP wise stat from VCF
9.6 years ago by Jorge Amigo 14k
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2.6k
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Answer: A: Any tool to get SNP wise stat from VCF
9.6 years ago by Jorge Amigo 14k
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Comment: C: Bcftools equivalent of vcf-merge R?
9.6 years ago by Jorge Amigo 14k
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6.1k
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Comment: C: Print all rows that are in specified value range based on specific column as pai
9.6 years ago by Jorge Amigo 14k
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1
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6.1k
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Comment: C: Print all rows that are in specified value range based on specific column as pai
9.6 years ago by Jorge Amigo 14k
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6.1k
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Comment: C: Print all rows that are in specified value range based on specific column as pai
9.6 years ago by Jorge Amigo 14k
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Comment: C: Coverage In Bam File - Bases And Overall Count
9.6 years ago by Jorge Amigo 14k
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6.1k
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Answer: A: Print all rows that are in specified value range based on specific column as pai
9.6 years ago by Jorge Amigo 14k
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4.4k
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Comment: C: 1000 GENOME RETRIEVE DATA
9.6 years ago by Jorge Amigo 14k
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39k
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Comment: C: New Fasta Sequence From Reference Fasta And Variant Calls File?
9.6 years ago by Jorge Amigo 14k
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1
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4.4k
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Comment: C: 1000 GENOME RETRIEVE DATA
9.6 years ago by Jorge Amigo 14k
3
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4.4k
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Answer: A: 1000 GENOME RETRIEVE DATA
9.6 years ago by Jorge Amigo 14k
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39k
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Comment: C: New Fasta Sequence From Reference Fasta And Variant Calls File?
9.6 years ago by Jorge Amigo 14k
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2.1k
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Comment: C: How to remove the last character "," from each row in bed file?
9.6 years ago by Jorge Amigo 14k
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Answer: A: How to remove the last character "," from each row in bed file?
9.6 years ago by Jorge Amigo 14k
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9.6k
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Comment: C: Finding a specific gene in a fastq file without mapping the reads?
9.6 years ago by Jorge Amigo 14k
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1
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7.9k
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Answer: A: Error while trying to get consensus Fastq from BAM
9.6 years ago by Jorge Amigo 14k
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7.9k
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Answer: A: Error while trying to get consensus Fastq from BAM
9.6 years ago by Jorge Amigo 14k
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7.9k
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Comment: C: Error while trying to get consensus Fastq from BAM
9.6 years ago by Jorge Amigo 14k
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2.4k
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Comment: C: Risk allele frequency via 1000 genome browser
9.6 years ago by Jorge Amigo 14k
1
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1.8k
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Answer: A: Counting reads per codon
9.6 years ago by Jorge Amigo 14k
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3.9k
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Answer: A: Missing alleles for a genotype in UYG VCF file
9.6 years ago by Jorge Amigo 14k
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4.9k
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Answer: A: Bcftools equivalent of vcf-merge R?
9.6 years ago by Jorge Amigo 14k
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47k
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Comment: C: Extract subset of samples from multigenome vcf file
9.6 years ago by Jorge Amigo 14k
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2.0k
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Comment: C: Significant difference between Grch37 and human_g1k_37
9.6 years ago by Jorge Amigo 14k
1
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1
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9.6k
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Comment: C: Finding specific gene in reads
9.6 years ago by Jorge Amigo 14k
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1
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9.6k
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Comment: C: Finding specific gene in reads
9.6 years ago by Jorge Amigo 14k
5
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9.6k
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Answer: A: Finding specific gene in reads
9.6 years ago by Jorge Amigo 14k
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3.6k
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Comment: C: why is this example homozygous 0/0 ?
9.6 years ago by Jorge Amigo 14k
3
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3.6k
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Answer: A: why is this example homozygous 0/0 ?
9.6 years ago by Jorge Amigo 14k
1
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1
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47k
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Comment: C: Extract subset of samples from multigenome vcf file
9.6 years ago by Jorge Amigo 14k
1
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7.6k
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Comment: C: How to interpret and extract from a Vcf file Genotype informations as values
9.6 years ago by Jorge Amigo 14k
1
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1
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7.6k
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Comment: C: How to interpret and extract from a Vcf file Genotype informations as values
9.6 years ago by Jorge Amigo 14k
12
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47k
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Answer: A: Extract subset of samples from multigenome vcf file
9.6 years ago by Jorge Amigo 14k
0
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2.7k
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Answer: A: convert2annovar Skipped invalid alternative alleles found in input file
9.7 years ago by Jorge Amigo 14k
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0
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4.0k
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Comment: C: Combine multiple vcf (or gVCF) from Ion Torrent
9.9 years ago by Jorge Amigo 14k
3
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1
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4.0k
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Answer: A: Combine multiple vcf (or gVCF) from Ion Torrent
9.9 years ago by Jorge Amigo 14k
5
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23k
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Answer: A: Gff Or Bed File For Hg19 Genome
9.9 years ago by Jorge Amigo 14k
12
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2
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43k
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Answer: A: Ti/Tv Ratio Confirms Snp Discovery. Is This A General Rule?
9.9 years ago by Jorge Amigo 14k
3
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3.6k
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Answer: A: How many SNPs are sufficiant for Sample identify uniquely?
10.0 years ago by Jorge Amigo 14k
1
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2.5k
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Comment: C: Same locus, more rs IDs
10.0 years ago by Jorge Amigo 14k
1
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1
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7.0k
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Answer: A: Counting number of bases covered across multiple bam files
10.0 years ago by Jorge Amigo 14k
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0
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6.3k
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Answer: A: How can I get .bed file that have unique Entrez gene id (or symbol) for deeptool
10.1 years ago by Jorge Amigo 14k
2
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3.1k
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Comment: C: Replace REF and ALT columns based on the GT of one sample in a VCF file
10.1 years ago by Jorge Amigo 14k
0
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0
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5.0k
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Comment: C: How to obtain ancestral alleles based on Hg19 genome coordinates?
10.1 years ago by Jorge Amigo 14k
884 results • Page 7 of 18
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