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2
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why is important to identify genetic risk variants?
genetic risk variants
updated 20 months ago by 84k • written 20 months ago by • 0
0
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1
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558
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How to build my resource-bundle for variant recalibrator?
Resource Bundle
updated 2.5 years ago by ▴ 90 • written 3.3 years ago by • 0
0
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1
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783
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Comment: C: Analyzing VCF file
3.6 years ago by Sakhaa • 0
1
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5
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783
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Analyzing VCF file
SNP sequence next-gen genome
3.6 years ago by Sakhaa • 0
0
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0
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783
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Comment: A: Analyzing VCF file
3.6 years ago by Sakhaa • 0
0
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1
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2.9k
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How to convert g.vcf to .vcf file
genome sequence alignment tool vcf
3.9 years ago by Sakhaa • 0
0
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2
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3.9k
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Comment: C: Question: Converting FASTQ to BAM by using Bowtie2
4.0 years ago by Sakhaa • 0
2
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8
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3.9k
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Question: Converting FASTQ to BAM by using Bowtie2
alignment sequencing SNP genome
updated 4.0 years ago by 97k • written 4.0 years ago by • 0
5
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3
replies
2.4k
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Extracting a special chromosome in fastq file
alignment sequencing genome sequence gene
4.1 years ago by Sakhaa • 0
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