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Comment: C: How to identify monomorphic snp position
9.0 years ago by Jorge Amigo 14k
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Comment: C: How to identify monomorphic snp position
9.0 years ago by Jorge Amigo 14k
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Answer: A: How to identify monomorphic snp position
9.0 years ago by Jorge Amigo 14k
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8.3k
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Comment: C: How to identify monomorphic snp position
9.0 years ago by Jorge Amigo 14k
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8.3k
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Comment: C: How to identify monomorphic snp position
9.0 years ago by Jorge Amigo 14k
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Comment: C: Awk or Shell script in need
9.0 years ago by Jorge Amigo 14k
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3.9k
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Comment: C: Awk or Shell script in need
9.0 years ago by Jorge Amigo 14k
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8.3k
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Comment: C: How to identify monomorphic snp position
9.0 years ago by Jorge Amigo 14k
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4.0k
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Comment: C: Extract Information from fasta File
9.0 years ago by Jorge Amigo 14k
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Answer: A: String research in a fasta file
9.0 years ago by Jorge Amigo 14k
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6.0k
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Comment: C: String research in a fasta file
9.0 years ago by Jorge Amigo 14k
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6.0k
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Comment: C: String research in a fasta file
9.0 years ago by Jorge Amigo 14k
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14k
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Answer: A: remove a list of positions form a vcf file
9.0 years ago by Jorge Amigo 14k
7
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4.1k
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Answer: A: Is there a tool that can output the raw genotype call (i.e., 0/1) rather than th
9.0 years ago by Jorge Amigo 14k
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2.1k
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Comment: C: Determining length of numerical ranges in file by perl/awk
9.0 years ago by Jorge Amigo 14k
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3
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2.1k
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Comment: C: Determining length of numerical ranges in file by perl/awk
9.0 years ago by Jorge Amigo 14k
2
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1
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2.1k
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Answer: A: Determining length of numerical ranges in file by perl/awk
9.0 years ago by Jorge Amigo 14k
2
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4.1k
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Answer: A: Converting Bedgraph to coverage
9.0 years ago by Jorge Amigo 14k
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2.1k
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Answer: A: FASTA sequence modification
9.0 years ago by Jorge Amigo 14k
1
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1
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11k
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Answer: A: Extracting specific SNPs from vcf file
9.1 years ago by Jorge Amigo 14k
2
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8.8k
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Answer: A: Genotype count in a VCF file
9.1 years ago by Jorge Amigo 14k
2
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4.1k
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Answer: A: How to summarize variant data in multiple VCF files?
9.1 years ago by Jorge Amigo 14k
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3.4k
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Comment: C: Converting genotype data to SNP calls
9.1 years ago by Jorge Amigo 14k
2
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1
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3.4k
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Answer: A: Converting genotype data to SNP calls
9.1 years ago by Jorge Amigo 14k
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1
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5.9k
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Comment: C: How to create ID field in vcf with vcftools
9.2 years ago by Jorge Amigo 14k
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2.7k
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Comment: C: merge two mulitfasta files and eliminate fasta with duplicated headers from the
9.4 years ago by Jorge Amigo 14k
2
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1
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2.7k
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Answer: A: merge two mulitfasta files and eliminate fasta with duplicated headers from the
9.4 years ago by Jorge Amigo 14k
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2.0k
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Answer: A: problem in annotate my vcf file to SNPdb files or another vcf file ??
9.4 years ago by Jorge Amigo 14k
2
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1
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5.6k
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Answer: A: Converting Thousand genome BCF file into VCF with BCFtools
9.4 years ago by Jorge Amigo 14k
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1
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1.6k
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Answer: C: how is 1000g vcf generated ? call variants through all samples together or seper
9.4 years ago by Jorge Amigo 14k
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1.7k
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Comment: C: How to subset the fasta sequence starting with "G"?
9.4 years ago by Jorge Amigo 14k
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0
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1.7k
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Answer: C: How to subset the fasta sequence starting with "G"?
9.4 years ago by Jorge Amigo 14k
1
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2.0k
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Answer: A: Find number of reads that contain at least 1 sequence from a list of sequences
9.4 years ago by Jorge Amigo 14k
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0
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6.1k
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Comment: C: BamTobw bedGraphToBigWig: command not found
9.5 years ago by Jorge Amigo 14k
1
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0
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3.6k
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Answer: A: Difference of samtools depth count and samtools tview count
9.5 years ago by Jorge Amigo 14k
1
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2.4k
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Comment: C: Is there any GUI tool which can compare 200 VCFs and show different SNPs between
9.5 years ago by Jorge Amigo 14k
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0
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7.8k
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Comment: C: How do I remove polymorphisms that failed filtering from a vcf file?
9.5 years ago by Jorge Amigo 14k
1
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1
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7.8k
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Answer: A: How do I remove polymorphisms that failed filtering from a vcf file?
9.5 years ago by Jorge Amigo 14k
2
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0
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3.3k
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Answer: A: Reads in BAM file overlapping coordinates
9.5 years ago by Jorge Amigo 14k
3
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0
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4.5k
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Comment: C: depth calculation for targeted resequencing
9.5 years ago by Jorge Amigo 14k
1
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1
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5.3k
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Answer: A: How to find the insertion sequence in .bam file?
9.5 years ago by Jorge Amigo 14k
6
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0
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4.5k
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Answer: A: depth calculation for targeted resequencing
9.5 years ago by Jorge Amigo 14k
0
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0
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5.2k
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Comment: C: Splitting fastq from stdin into multiple files ?
9.5 years ago by Jorge Amigo 14k
0
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0
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4.2k
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Comment: C: awk : if length to a pattern at column 2 is less than 5
9.5 years ago by Jorge Amigo 14k
3
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2
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4.2k
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Answer: A: awk : if length to a pattern at column 2 is less than 5
9.5 years ago by Jorge Amigo 14k
1
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0
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3.0k
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Comment: C: bowtie2 output only valid alignments
9.5 years ago by Jorge Amigo 14k
10
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11k
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Answer: A: 1/2 in VCF genotype field?
9.5 years ago by Jorge Amigo 14k
0
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0
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3.2k
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Comment: C: VCF isnot compressed and indexed even after running bgzip and tabix,
9.5 years ago by Jorge Amigo 14k
1
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1
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5.2k
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Answer: A: Splitting fastq from stdin into multiple files ?
9.5 years ago by Jorge Amigo 14k
1
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0
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2.3k
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Answer: A: Output AO using bcftools
9.5 years ago by Jorge Amigo 14k
884 results • Page 6 of 18
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