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Comment: Comment: Why are some WES VCFs larger than others?
4 months ago by Prash ▴ 190
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Comment: Comment: Pan genome based assembly
4 months ago by Prash ▴ 190
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Comment: Comment: How many basepairs are genes padded by in WES?
7 months ago by Prash ▴ 190
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Comment: Comment: Paired - end sequencing
8 months ago by Prash ▴ 190
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Comment: Comment: Advice on how to generate synthetic Copy Number Variation data
11 months ago by Prash ▴ 190
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Comment: Comment: NGS Sequence quality
11 months ago by Prash ▴ 190
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Comment: Comment: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
12 months ago by Prash ▴ 190
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Comment: Comment: Commercial software for genomics / NGS / bioinformatics
13 months ago by Prash ▴ 190
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2.3k
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Comment: Comment: How to filter SNPs with excess heterozygosity from a large vcf
14 months ago by Prash ▴ 190
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Comment: Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
17 months ago by Prash ▴ 190
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Comment: Comment: Error with per tile sequence quality (by FastQC)
17 months ago by Prash ▴ 190
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Comment: Comment: Variant Allele frequency
18 months ago by Prash ▴ 190
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Comment: Comment: When to merge BAM or SAM files?
18 months ago by Prash ▴ 190
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