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Answer: Answer: Bioinformatics variant calling software
7 months ago by Charles Yin ▴ 180
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1.1k
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Comment: Comment: get SNPs from draft genomes
22 months ago by Charles Yin ▴ 180
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1.1k
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Answer: Answer: get SNPs from draft genomes
22 months ago by Charles Yin ▴ 180
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2.8k
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Comment: C: paired-end reads in BBMap randomreads.sh
5.8 years ago by Charles Yin ▴ 180
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1
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1.7k
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Answer: A: Identifying shared exact sequence variants between two datasets
5.9 years ago by Charles Yin ▴ 180
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1
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3.8k
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Comment: C: SNP analysis between two bacterial genomes
6.0 years ago by Charles Yin ▴ 180
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4.0k
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Answer: A: How can I contribute to the Bioinformatics community as a Software Engineer
6.1 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
6.3 years ago by Charles Yin ▴ 180
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2
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1.1k
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how to determine bacteria relatedness from two variant calls
next-gen genome SNP
updated 6.3 years ago by 6.1k • written 6.3 years ago by ▴ 180
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2
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2.5k
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can variants be called between two genomes?
SNP alignment next-gen sequence
6.4 years ago by Charles Yin ▴ 180
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2.5k
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Answer: A: can variants be called between two genomes?
6.4 years ago by Charles Yin ▴ 180
3
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3
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5.2k
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Working example for VCF visualization in Circos
SNP next-gen
updated 6.8 years ago by • 0 • written 7.3 years ago by ▴ 180
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4.1k
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Comment: A: Number of SNPs in VCF
7.0 years ago by Charles Yin ▴ 180
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1
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4.3k
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Comment: C: SNP density plot
7.1 years ago by Charles Yin ▴ 180
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1
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2.8k
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Phylogenetic tree visualization by Python
sequence genome
7.1 years ago by Charles Yin ▴ 180
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0
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2.8k
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Answer: A: Phylogenetic tree visualization by Python
7.1 years ago by Charles Yin ▴ 180
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3
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1.6k
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How to validate zero SNPs in variant calling?
SNP alignment
updated 7.1 years ago by 20 • written 7.2 years ago by ▴ 180
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3.5k
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Answer: A: Bioinformatics independent research group
7.2 years ago by Charles Yin ▴ 180
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3.5k
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Comment: C: Bioinformatics independent research group
7.2 years ago by Charles Yin ▴ 180
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1
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3.5k
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Comment: C: Bioinformatics independent research group
7.2 years ago by Charles Yin ▴ 180
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1
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3.5k
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Comment: C: Bioinformatics independent research group
7.2 years ago by Charles Yin ▴ 180
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3.5k
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Comment: C: Bioinformatics independent research group
7.2 years ago by Charles Yin ▴ 180
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1
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3.5k
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Comment: A: Bioinformatics independent research group
7.2 years ago by Charles Yin ▴ 180
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1
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1.6k
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Comment: C: How to validate zero SNPs in variant calling?
7.2 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?
7.2 years ago by Charles Yin ▴ 180
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2
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2.0k
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How to know which reads were not aligned to a reference genome?
sequence SNP alignmet
updated 7.2 years ago by ★ 3.0k • written 7.2 years ago by ▴ 180
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2.7k
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Comment: C: Is it possible to get VCF from two fastq files without reference genome?
7.2 years ago by Charles Yin ▴ 180
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1
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2.7k
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Comment: C: Is it possible to get VCF from two fastq files without reference genome?
7.2 years ago by Charles Yin ▴ 180
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1
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2.7k
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Comment: C: Is it possible to get VCF from two fastq files without reference genome?
7.2 years ago by Charles Yin ▴ 180
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0
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2.7k
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Comment: C: Is it possible to get VCF from two fastq files without reference genome?
7.2 years ago by Charles Yin ▴ 180
2
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8
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2.7k
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Is it possible to get VCF from two fastq files without reference genome?
next-gen snp
updated 7.2 years ago by 7.4k • written 7.2 years ago by ▴ 180
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9.9k
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Comment: A: Truncated sam file - Parse error
7.2 years ago by Charles Yin ▴ 180
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1
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5.2k
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Answer: C: Working example for VCF visualization in Circos
7.3 years ago by Charles Yin ▴ 180
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9.0k
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Comment: C: How to display mismatched sequences from alignment when using Biopython
7.3 years ago by Charles Yin ▴ 180
7
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17
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9.0k
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6 follow
How to display mismatched sequences from alignment when using Biopython
alignment biopython
updated 7.3 years ago by ★ 2.7k • written 7.3 years ago by ▴ 180
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2
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9.0k
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Comment: C: How to display mismatched sequences from alignment when using Biopython
7.3 years ago by Charles Yin ▴ 180
1
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3
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9.0k
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Comment: C: How to display mismatched sequences from alignment when using Biopython
7.3 years ago by Charles Yin ▴ 180
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0
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9.0k
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Comment: C: How to display mismatched sequences from alignment when using Biopython
7.3 years ago by Charles Yin ▴ 180
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2
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9.0k
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Comment: C: How to display mismatched sequences from alignment when using Biopython
7.3 years ago by Charles Yin ▴ 180
2
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0
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1.7k
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Answer: A: Phylogeny Analysis Data
7.4 years ago by Charles Yin ▴ 180
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1
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1.4k
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Answer: A: human gut microbiota with disease and drug resistance
7.6 years ago by Charles Yin ▴ 180
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1
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1.9k
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Answer: A: Method of Checking for Mutation Patterns
7.6 years ago by Charles Yin ▴ 180
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1
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2.5k
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Comment: A: How to get list of GenBank accession Ids by a Taxonomy Id?
7.7 years ago by Charles Yin ▴ 180
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3
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2.5k
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How to get list of GenBank accession Ids by a Taxonomy Id?
sequence Genbank
7.7 years ago by Charles Yin ▴ 180
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0
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5.1k
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Answer: A: Copy Number Variation Tools
7.7 years ago by Charles Yin ▴ 180
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1.4k
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Answer: A: Comparative analysis, genomic analysis of infectious bacteria
7.7 years ago by Charles Yin ▴ 180
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0
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2.5k
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Comment: C: Recommendations about phylogenetic analysis tools for RFLP/AFLP/RAPD data
7.7 years ago by Charles Yin ▴ 180
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0
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1.7k
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Answer: A: How can i do this by matlab ??
updated 7.7 years ago by 147k • written 7.7 years ago by ▴ 180
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1.7k
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Answer: A: How can i do this by matlab ??
updated 7.7 years ago by 147k • written 7.7 years ago by ▴ 180
0
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1
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2.5k
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Answer: A: Recommendations about phylogenetic analysis tools for RFLP/AFLP/RAPD data
7.7 years ago by Charles Yin ▴ 180
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