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Answer:
C: What is the significance of this file in COSMIC database?
5.5 years ago by
Titus
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Answer:
C: SNPs annotations tool
5.6 years ago by
Titus
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A: Why is HGVS notation not available for some variants?
5.6 years ago by
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C: 20 millions reads per sample for SNP
6.2 years ago by
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C: SNP single end read
6.2 years ago by
Titus
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C: VEP and Annovar Annotation
6.7 years ago by
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Answer:
C: How can I transform CNV output data of Agilent 244K to TCGA/GDC data?
6.8 years ago by
Titus
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Answer:
C: How to annotate the Bacterial genome VCF ?
6.9 years ago by
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Answer:
C: How to draw circular plot to show genomewide snps and indels distribution?
6.9 years ago by
Titus
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Answer:
C: Reason for multiple mapping of reads ?
6.9 years ago by
Titus
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Answer:
C: where to find a list of often mutated or lost regions in cancers
7.0 years ago by
Titus
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Answer:
C: finding homologs in human
7.0 years ago by
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Answer:
A: Copy Number Variation Tools
7.0 years ago by
Titus
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Answer:
A: igvtools count - how do I get it to show insertion and deletion count
7.1 years ago by
Titus
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