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Add dbSNP identifiers to PLINK output
SNP next-gen sequencing
5.2 years ago by Tash • 0
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Comment: C: DESeq2 using samples with different unique alignment rates
7.1 years ago by Tash • 0
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Comment: C: DESeq2 using samples with different unique alignment rates
7.1 years ago by Tash • 0
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1.9k
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DESeq2 using samples with different unique alignment rates
RNA-Seq R
7.1 years ago by Tash • 0
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1.8k
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Comment: C: Identifying enriched pathways that overlap among a range of databases
7.6 years ago by Tash • 0
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Identifying enriched pathways that overlap among a range of databases
next-gen
updated 7.6 years ago by ★ 3.2k • written 7.6 years ago by • 0
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Single rare variant approaches
next-gen
updated 7.6 years ago by ▴ 960 • written 7.6 years ago by • 0
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Comment: C: Single rare variant approaches
7.6 years ago by Tash • 0
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