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Add dbSNP identifiers to PLINK output
SNP next-gen sequencing
4.4 years ago by Tash • 0
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Comment: C: DESeq2 using samples with different unique alignment rates
6.3 years ago by Tash • 0
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Comment: C: DESeq2 using samples with different unique alignment rates
6.3 years ago by Tash • 0
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1.6k
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DESeq2 using samples with different unique alignment rates
RNA-Seq R
6.3 years ago by Tash • 0
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1.5k
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Comment: C: Identifying enriched pathways that overlap among a range of databases
6.7 years ago by Tash • 0
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2
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Identifying enriched pathways that overlap among a range of databases
next-gen
updated 6.7 years ago by ★ 3.1k • written 6.7 years ago by • 0
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4.2k
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Single rare variant approaches
next-gen
updated 6.7 years ago by ▴ 960 • written 6.7 years ago by • 0
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Comment: C: Single rare variant approaches
6.7 years ago by Tash • 0
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