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Answer: Answer: Protein prediction tool
3.6 years ago by Collin ▴ 1000
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Answer: Answer: Can non-driver mutations disrupt the function of proteins and further affect a c
3.7 years ago by Collin ▴ 1000
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2.8k
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Answer: Answer: Identification of transcription factors from a list of DEGs
3.8 years ago by Collin ▴ 1000
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Answer: Answer: Association analysis with SNP
3.8 years ago by Collin ▴ 1000
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Answer: Answer: Preparing CHASMplus database for annotation
3.9 years ago by Collin ▴ 1000
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Answer: A: Is there a tool to predict if a missense variant causes a loss of function on th
updated 4.2 years ago by 151k • written 4.4 years ago by ▴ 1000
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Answer: Answer: SNP annotation tool
updated 3.3 years ago by 45k • written 4.5 years ago by ▴ 1000
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Answer: C: TCGA driver mutation data
4.5 years ago by Collin ▴ 1000
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5.9k
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Answer: C: Get clinVar info for SNP with VEP
5.0 years ago by Collin ▴ 1000
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1.8k
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Answer: A: How to download passenger mutations for cancer
5.2 years ago by Collin ▴ 1000
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Answer: A: Getting a list of tumor suppressors
5.2 years ago by Collin ▴ 1000
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4.3k
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Answer: A: Can't open file 'features': [Errno 2] No such file or directory
5.2 years ago by Collin ▴ 1000
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1.5k
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Answer: A: Cancer driver mutations Identification from VCFs
5.3 years ago by Collin ▴ 1000
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Answer: A: about snp prediction
5.3 years ago by Collin ▴ 1000
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1.4k
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Answer: A: Somatic Variant Annotation and Interpretation
5.3 years ago by Collin ▴ 1000
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5.1k
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Answer: A: Indel Annotation Tools, Not Loss Of Function
5.4 years ago by Collin ▴ 1000
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5.4k
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Answer: A: How to "merge" monomeric structures in COOT (WinCoot) - pdb files
updated 5.4 years ago by 45k • written 9.4 years ago by ▴ 1000
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3.0k
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Answer: A: Are there certain mutations ubiquitous in ALL cancers?
updated 5.5 years ago by 45k • written 9.5 years ago by ▴ 1000
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20k
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Answer: A: Benjamini+ Hochberg multiple testing p.adjust R
6.9 years ago by Collin ▴ 1000
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1
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2.9k
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Answer: A: Constructing a mean ROC curve based on 5 iterations
6.9 years ago by Collin ▴ 1000
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1.4k
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Answer: A: Alternative tools replace MutDB to predict consequences of deleterious SNV
7.3 years ago by Collin ▴ 1000
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2.2k
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Answer: A: 2020+ installation problems:
7.5 years ago by Collin ▴ 1000
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1.9k
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Answer: A: Input file requirements for hg38
7.6 years ago by Collin ▴ 1000
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2.5k
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Answer: A: BRCA1 and BRCA2 database's for NGS diagnostics purposes
7.7 years ago by Collin ▴ 1000
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2.9k
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Answer: A: Statistical test for finding driver mutations.
8.1 years ago by Collin ▴ 1000
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4.6k
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Answer: A: How to conduct pathway analysis from VCF file?
8.3 years ago by Collin ▴ 1000
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10k
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Answer: C: Effect size of a SNP - contribution to genetic variance
8.5 years ago by Collin ▴ 1000
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Answer: A: User Friendly VCF Filtering Tools
9.0 years ago by Collin ▴ 1000
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14k
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Answer: Answer: Map genetic mutations to protein domain/structure
updated 3.2 years ago by 45k • written 9.0 years ago by ▴ 1000
3
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2.6k
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Answer: A: Difficulty replicating likelihood ratio test from RNA-seq paper
9.1 years ago by Collin ▴ 1000
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1
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2.1k
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Answer: A: COSMIC data and rare variant
9.2 years ago by Collin ▴ 1000
2
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0
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16k
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Answer: Answer: Best Graphics Gallery Or Blogs For Bioinformatics Use
updated 2.8 years ago by 45k • written 9.3 years ago by ▴ 1000
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