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Answer: Answer: Protein prediction tool
4.1 years ago by Collin ▴ 1000
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Comment: Comment: Can non-driver mutations disrupt the function of proteins and further affect a c
4.2 years ago by Collin ▴ 1000
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Comment: Comment: Can non-driver mutations disrupt the function of proteins and further affect a c
4.2 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
4.2 years ago by Collin ▴ 1000
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Answer: Answer: Identification of transcription factors from a list of DEGs
4.2 years ago by Collin ▴ 1000
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Answer: Answer: Association analysis with SNP
4.3 years ago by Collin ▴ 1000
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Comment: Comment: Preparing CHASMplus database for annotation
4.3 years ago by Collin ▴ 1000
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Comment: Comment: Preparing CHASMplus database for annotation
4.3 years ago by Collin ▴ 1000
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Answer: Answer: Preparing CHASMplus database for annotation
4.3 years ago by Collin ▴ 1000
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7.8k
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Comment: Comment: Good annotation databases for a VCF file (somatic variants)
4.4 years ago by Collin ▴ 1000
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Comment: Comment: Good annotation databases for a VCF file (somatic variants)
4.4 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 4.7 years ago by 154k • written 4.9 years ago by ▴ 1000
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Comment: C: VEP is very slow. Fork doesnt seem to work
4.7 years ago by Collin ▴ 1000
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5.2k
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Comment: C: VEP is very slow. Fork doesnt seem to work
4.7 years ago by Collin ▴ 1000
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Comment: C: Is there a tool to predict if a missense variant causes a loss of function on th
4.9 years ago by Collin ▴ 1000
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Answer: Answer: SNP annotation tool
updated 3.8 years ago by 45k • written 5.0 years ago by ▴ 1000
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3.1k
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Comment: C: TCGA driver mutation data
5.0 years ago by Collin ▴ 1000
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Comment: C: Protein_Change in MAF
5.0 years ago by Collin ▴ 1000
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Comment: C: TCGA driver mutation data
5.0 years ago by Collin ▴ 1000
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3.1k
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Comment: C: TCGA driver mutation data
5.0 years ago by Collin ▴ 1000
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3.1k
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Comment: C: TCGA driver mutation data
5.0 years ago by Collin ▴ 1000
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3.1k
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Comment: C: TCGA driver mutation data
5.0 years ago by Collin ▴ 1000
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Answer: C: TCGA driver mutation data
5.0 years ago by Collin ▴ 1000
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1.8k
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Comment: C: Variant Calling scRNA-seq data for KRAS mutations
5.1 years ago by Collin ▴ 1000
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1.8k
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Comment: C: Variant Calling scRNA-seq data for KRAS mutations
5.1 years ago by Collin ▴ 1000
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Comment: C: Get clinVar info for SNP with VEP
5.5 years ago by Collin ▴ 1000
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7.8k
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Comment: C: Get clinVar info for SNP with VEP
5.5 years ago by Collin ▴ 1000
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7.8k
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Answer: C: Get clinVar info for SNP with VEP
5.5 years ago by Collin ▴ 1000
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1.5k
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Comment: C: Variant effect prediction
5.5 years ago by Collin ▴ 1000
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Comment: C: How to go from VCF file to protein level
5.5 years ago by Collin ▴ 1000
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1.6k
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Comment: C: Mutation clustering in protein domains
5.6 years ago by Collin ▴ 1000
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Comment: C: How to download passenger mutations for cancer
5.7 years ago by Collin ▴ 1000
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Comment: C: How to download passenger mutations for cancer
5.7 years ago by Collin ▴ 1000
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2.3k
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Answer: A: How to download passenger mutations for cancer
5.7 years ago by Collin ▴ 1000
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Tool: CRAVAT: a web tool to annotate and analyze cancer variants
sequencing variant annotation Cancer
updated 3.7 years ago by 45k • written 10.0 years ago by ▴ 1000
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Answer: A: Getting a list of tumor suppressors
5.7 years ago by Collin ▴ 1000
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4.6k
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Comment: C: Can't open file 'features': [Errno 2] No such file or directory
5.7 years ago by Collin ▴ 1000
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4.6k
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Answer: A: Can't open file 'features': [Errno 2] No such file or directory
5.7 years ago by Collin ▴ 1000
2
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1.8k
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Answer: A: Cancer driver mutations Identification from VCFs
5.7 years ago by Collin ▴ 1000
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Comment: C: Suggested tool or algorithm for accessing pathogenicity and prioritization of so
5.7 years ago by Collin ▴ 1000
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1.7k
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Comment: C: Suggested tool or algorithm for accessing pathogenicity and prioritization of so
5.7 years ago by Collin ▴ 1000
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Comment: C: Interesting things to do with 23andme data
5.7 years ago by Collin ▴ 1000
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920
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Answer: A: about snp prediction
5.7 years ago by Collin ▴ 1000
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1.7k
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Answer: A: Somatic Variant Annotation and Interpretation
5.8 years ago by Collin ▴ 1000
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5.6k
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Answer: A: Indel Annotation Tools, Not Loss Of Function
5.9 years ago by Collin ▴ 1000
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5.9k
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Answer: A: How to "merge" monomeric structures in COOT (WinCoot) - pdb files
updated 5.9 years ago by 45k • written 9.9 years ago by ▴ 1000
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3.5k
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Answer: A: Are there certain mutations ubiquitous in ALL cancers?
updated 5.9 years ago by 45k • written 9.9 years ago by ▴ 1000
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Comment: C: pathogenicity predictors of cancer mutations
6.3 years ago by Collin ▴ 1000
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Comment: C: Which Driver-Gene Detecting Software Supports hg38?
6.3 years ago by Collin ▴ 1000
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6.1k
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Comment: C: Which Driver-Gene Detecting Software Supports hg38?
6.3 years ago by Collin ▴ 1000
120 results • Page 1 of 3
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