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nchuang • 200
Status: New
Handle: @nchuang18948
Reputation: 200
Joined: 19 months ago
Last seen: 2.3 years ago
Location: United States

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Comment: C: CpG Methylation data from PacBio sequencing
2.3 years ago
nchuang • 200
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311
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Comment: C: CpG Methylation data from PacBio sequencing
2.3 years ago
nchuang • 200
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1.1k
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Comment: C: VIew reads sorted by name in IGV
3.3 years ago
nchuang • 200
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1.1k
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Comment: C: VIew reads sorted by name in IGV
3.3 years ago
nchuang • 200
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1.1k
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Comment: C: VIew reads sorted by name in IGV
3.3 years ago
nchuang • 200
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961
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Comment: C: Edit a single base in SeqRecord object in Biopython?
4.1 years ago
nchuang • 200
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883
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Comment: C: Popen Blat has different behavior than same syntax in shell
4.3 years ago
nchuang • 200
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883
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Comment: C: Popen Blat has different behavior than same syntax in shell
4.3 years ago
nchuang • 200
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883
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Comment: C: Popen Blat has different behavior than same syntax in shell
4.3 years ago
nchuang • 200
1
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883
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Comment: C: Popen Blat has different behavior than same syntax in shell
4.3 years ago
nchuang • 200
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905
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Comment: C: Can NUCmer align a short sequence with a much longer sequence (local alignment)?
4.4 years ago
nchuang • 200
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949
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Comment: C: Fast way to extract hg19 sequences with Biopython?
4.6 years ago
nchuang • 200
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949
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Comment: C: Fast way to extract hg19 sequences with Biopython?
4.6 years ago
nchuang • 200
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1.2k
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Comment: C: Using a Multiple Seq Alignment tool for pairwise alignments possible?
4.7 years ago
nchuang • 200
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777
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Comment: C: How to visualize a set of sequence alignments that all have the same reference s
4.7 years ago
nchuang • 200
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952
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Comment: C: Substitution matrices to score variation between protein sequences?
4.7 years ago
nchuang • 200
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1
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777
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Comment: C: How to visualize a set of sequence alignments that all have the same reference s
4.7 years ago
nchuang • 200
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1.2k
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Comment: C: Using a Multiple Seq Alignment tool for pairwise alignments possible?
4.7 years ago
nchuang • 200
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1.4k
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Comment: C: How to create empty Biopython MultipleSeqAlignment object?
4.8 years ago
nchuang • 200
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1.4k
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Comment: C: How to create empty Biopython MultipleSeqAlignment object?
4.8 years ago
nchuang • 200
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1.4k
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Comment: C: How to create empty Biopython MultipleSeqAlignment object?
4.8 years ago
nchuang • 200
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899
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Comment: C: LRE3 Retrotransposon sequence
4.9 years ago
nchuang • 200
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899
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Comment: C: LRE3 Retrotransposon sequence
4.9 years ago
nchuang • 200
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1
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899
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Comment: C: LRE3 Retrotransposon sequence
4.9 years ago
nchuang • 200
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5.9k
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Comment: C: Best way to convert VCF to PLINK file format and merge chromosomes?
5.4 years ago
nchuang • 200
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5.9k
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Comment: C: Best way to convert VCF to PLINK file format and merge chromosomes?
5.4 years ago
nchuang • 200
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1
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5.9k
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Comment: C: Best way to convert VCF to PLINK file format and merge chromosomes?
5.4 years ago
nchuang • 200
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5.5k
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Comment: C: GWAS: when is it appropriate to add covariates?
5.4 years ago
nchuang • 200
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1
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2.4k
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Comment: C: Hardy-Weinberg assumptions in variant calling
5.5 years ago
nchuang • 200
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2.4k
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Comment: C: Hardy-Weinberg assumptions in variant calling
5.5 years ago
nchuang • 200
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2.0k
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Comment: C: GATK jointgenotyping file locking and too many open files woes
5.5 years ago
nchuang • 200
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2.0k
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Comment: C: GATK jointgenotyping file locking woes
5.5 years ago
nchuang • 200
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2.0k
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Comment: C: GATK jointgenotyping file locking woes
5.5 years ago
nchuang • 200
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5.0k
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Comment: C: How to count SNPs, InDels
5.5 years ago
nchuang • 200
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5.0k
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Comment: C: How to count SNPs, InDels
5.5 years ago
nchuang • 200
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11k
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Comment: C: Count Of Variants
5.5 years ago
nchuang • 200
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