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Comment: Comment: Need help understanding core SNPs
7 weeks ago by Prash ▴ 280
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Comment: Comment: Why are some WES VCFs larger than others?
11 months ago by Prash ▴ 280
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Comment: Comment: Pan genome based assembly
12 months ago by Prash ▴ 280
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Comment: Comment: How many basepairs are genes padded by in WES?
15 months ago by Prash ▴ 280
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Comment: Comment: Paired - end sequencing
16 months ago by Prash ▴ 280
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775
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Comment: Comment: Advice on how to generate synthetic Copy Number Variation data
19 months ago by Prash ▴ 280
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1.7k
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Comment: Comment: NGS Sequence quality
19 months ago by Prash ▴ 280
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Comment: Comment: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
19 months ago by Prash ▴ 280
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2.9k
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Comment: Comment: Commercial software for genomics / NGS / bioinformatics
20 months ago by Prash ▴ 280
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3.2k
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Comment: Comment: How to filter SNPs with excess heterozygosity from a large vcf
21 months ago by Prash ▴ 280
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1.6k
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Comment: Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
2.1 years ago by Prash ▴ 280
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2.5k
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Comment: Comment: Error with per tile sequence quality (by FastQC)
2.1 years ago by Prash ▴ 280
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937
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Comment: Comment: Variant Allele frequency
2.1 years ago by Prash ▴ 280
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1.2k
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Comment: Comment: When to merge BAM or SAM files?
2.1 years ago by Prash ▴ 280
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