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Comment:
C: De-replicating sequence file after barcodes/primers removed.
5.6 years ago by
pfs
▴ 280
1
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1.5k
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Comment:
C: how to combain microarray sets from the same platform but raw data were normaliz
6.2 years ago by
pfs
▴ 280
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1.4k
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Comment:
C: Samtools mpileup ends abruptly without completing full analysis
6.2 years ago by
pfs
▴ 280
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1.2k
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Comment:
C: Given QTLs and genome annotation, quickly list genes closest to QTLs
6.3 years ago by
pfs
▴ 280
0
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1.9k
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Comment:
C: how to annotate chromosome position with the gene list file
6.3 years ago by
pfs
▴ 280
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6.6k
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Comment:
C: Stuck on calculating principal components
6.3 years ago by
pfs
▴ 280
0
votes
2
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6.6k
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Comment:
C: Stuck on calculating principal components
6.3 years ago by
pfs
▴ 280
0
votes
0
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1.4k
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Comment:
C: Indentical proteins but different Blast results
6.5 years ago by
pfs
▴ 280
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5.3k
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Comment:
C: Using Plink, get allele frequencies for a subset of individuals
6.5 years ago by
pfs
▴ 280
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2.8k
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Comment:
C: How to remove reads in a fastq file that DO NOT have adapter sequence in them?
6.6 years ago by
pfs
▴ 280
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1.5k
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Comment:
C: Any kind of sequences are AT-rich on the human genome
6.6 years ago by
pfs
▴ 280
0
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2
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1.5k
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Comment:
A: Normalization for NGS count data with high variance between observations / uneve
6.6 years ago by
pfs
▴ 280
0
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2.7k
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Comment:
C: HaplotypeCaller filter out variants covered only in one direction
6.6 years ago by
pfs
▴ 280
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