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How to annotate a VCF and convert it to a list of genes (names) with defined mutations?
annotation vcf
updated 7.8 years ago by ★ 5.2k • written 7.8 years ago by ▴ 10
4
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3
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2.8k
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How to install SAMTools and Gatk on CygWin and how to call it from Window`s Python and Java?
samtools gatk cygwin
7.8 years ago by flight22121 ▴ 10
1
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1.6k
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How to annotate VarScan software .snp output to see what genes have SNPs and how to make a human-readable report from that?
varscan annotation
7.8 years ago by flight22121 ▴ 10
0
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3
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1.4k
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What software tools can merge FASTQs and BAMs (SAMs) separately ?
bam fastqs wgs ngs
updated 7.8 years ago by ★ 2.9k • written 7.8 years ago by ▴ 10
0
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0
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1.7k
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Answer: A: How to run SNAP aligner on Windows correctly 10?
updated 7.8 years ago by 147k • written 7.8 years ago by ▴ 10
0
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5
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1.7k
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How to run SNAP aligner on Windows correctly 10?
snap sequencing alignment
7.8 years ago by flight22121 ▴ 10
0
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1
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1.7k
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Comment: C: How to run SNAP aligner on Windows correctly 10?
7.8 years ago by flight22121 ▴ 10
0
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1
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1.7k
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Comment: C: How to run SNAP aligner on Windows correctly 10?
updated 7.8 years ago by 147k • written 7.8 years ago by ▴ 10
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0
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1.3k
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Comment: C: How many paired FASTQ reads to input for alignment if 4 different SRA IDs belong
7.8 years ago by flight22121 ▴ 10
0
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3
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1.3k
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How many paired FASTQ reads to input for alignment if 4 different SRA IDs belong to one sample-whole genome?
sra alignment fastqs
updated 7.8 years ago by ▴ 360 • written 7.8 years ago by ▴ 10
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