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Comment: Comment: get SNPs from draft genomes
2.0 years ago by Charles Yin ▴ 180
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2.8k
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Comment: C: paired-end reads in BBMap randomreads.sh
6.0 years ago by Charles Yin ▴ 180
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3.8k
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Comment: C: SNP analysis between two bacterial genomes
6.2 years ago by Charles Yin ▴ 180
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1.1k
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Comment: C: how to determine bacteria relatedness from two variant calls
6.5 years ago by Charles Yin ▴ 180
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4.2k
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Comment: A: Number of SNPs in VCF
7.2 years ago by Charles Yin ▴ 180
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4.4k
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Comment: C: SNP density plot
7.3 years ago by Charles Yin ▴ 180
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3.8k
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Comment: C: Bioinformatics independent research group
7.4 years ago by Charles Yin ▴ 180
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1
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3.8k
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Comment: C: Bioinformatics independent research group
7.4 years ago by Charles Yin ▴ 180
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3.8k
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Comment: C: Bioinformatics independent research group
7.4 years ago by Charles Yin ▴ 180
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3.8k
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Comment: C: Bioinformatics independent research group
7.4 years ago by Charles Yin ▴ 180
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1
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3.8k
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Comment: A: Bioinformatics independent research group
7.4 years ago by Charles Yin ▴ 180
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1.7k
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Comment: C: How to validate zero SNPs in variant calling?
7.4 years ago by Charles Yin ▴ 180
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2.0k
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Comment: C: How to know which reads were not aligned to a reference genome?
7.5 years ago by Charles Yin ▴ 180
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2.8k
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Comment: C: Is it possible to get VCF from two fastq files without reference genome?
7.5 years ago by Charles Yin ▴ 180
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1
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2.8k
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Comment: C: Is it possible to get VCF from two fastq files without reference genome?
7.5 years ago by Charles Yin ▴ 180
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2.8k
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Comment: C: Is it possible to get VCF from two fastq files without reference genome?
7.5 years ago by Charles Yin ▴ 180
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2.8k
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Comment: C: Is it possible to get VCF from two fastq files without reference genome?
7.5 years ago by Charles Yin ▴ 180
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10k
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Comment: A: Truncated sam file - Parse error
7.5 years ago by Charles Yin ▴ 180
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9.3k
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Comment: C: How to display mismatched sequences from alignment when using Biopython
7.5 years ago by Charles Yin ▴ 180
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2
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9.3k
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Comment: C: How to display mismatched sequences from alignment when using Biopython
7.5 years ago by Charles Yin ▴ 180
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3
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9.3k
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Comment: C: How to display mismatched sequences from alignment when using Biopython
7.5 years ago by Charles Yin ▴ 180
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9.3k
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Comment: C: How to display mismatched sequences from alignment when using Biopython
7.5 years ago by Charles Yin ▴ 180
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2
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9.3k
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Comment: C: How to display mismatched sequences from alignment when using Biopython
7.5 years ago by Charles Yin ▴ 180
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1
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2.6k
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Comment: A: How to get list of GenBank accession Ids by a Taxonomy Id?
7.9 years ago by Charles Yin ▴ 180
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2.7k
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Comment: C: Recommendations about phylogenetic analysis tools for RFLP/AFLP/RAPD data
7.9 years ago by Charles Yin ▴ 180
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2.5k
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Comment: C: How to retrieve whole genome sequences by GenBank Ids
7.9 years ago by Charles Yin ▴ 180
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2.5k
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Comment: C: How to retrieve whole genome sequences by GenBank Ids
7.9 years ago by Charles Yin ▴ 180
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2.0k
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Comment: C: How to retrieve DNA sequence from GI number using Biopython?
7.9 years ago by Charles Yin ▴ 180
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