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Comment: Need help understanding core SNPs
5 days ago by
Prash
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1.4k
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Comment: Why are some WES VCFs larger than others?
10 months ago by
Prash
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1.9k
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Comment: Pan genome based assembly
10 months ago by
Prash
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613
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Comment: How many basepairs are genes padded by in WES?
13 months ago by
Prash
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Comment: Paired - end sequencing
14 months ago by
Prash
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Comment: Advice on how to generate synthetic Copy Number Variation data
17 months ago by
Prash
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Comment: NGS Sequence quality
17 months ago by
Prash
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2.1k
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Comment: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
18 months ago by
Prash
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2.7k
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Comment: Commercial software for genomics / NGS / bioinformatics
18 months ago by
Prash
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3.0k
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Comment: How to filter SNPs with excess heterozygosity from a large vcf
20 months ago by
Prash
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1.5k
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Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
23 months ago by
Prash
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2.3k
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Comment: Error with per tile sequence quality (by FastQC)
23 months ago by
Prash
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871
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Comment: Variant Allele frequency
24 months ago by
Prash
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Comment: When to merge BAM or SAM files?
24 months ago by
Prash
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