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Answer: Answer: Protein prediction tool
3.5 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
3.6 years ago by Collin ▴ 1000
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1.9k
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Comment: Comment: Can non-driver mutations disrupt the function of proteins and further affect a c
3.6 years ago by Collin ▴ 1000
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1.9k
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Answer: Answer: Can non-driver mutations disrupt the function of proteins and further affect a c
3.6 years ago by Collin ▴ 1000
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Answer: Answer: Identification of transcription factors from a list of DEGs
3.7 years ago by Collin ▴ 1000
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881
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Answer: Answer: Association analysis with SNP
3.8 years ago by Collin ▴ 1000
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1.8k
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Comment: Comment: Preparing CHASMplus database for annotation
3.8 years ago by Collin ▴ 1000
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1.8k
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Comment: Comment: Preparing CHASMplus database for annotation
3.8 years ago by Collin ▴ 1000
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1.8k
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Answer: Answer: Preparing CHASMplus database for annotation
3.8 years ago by Collin ▴ 1000
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6.4k
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Comment: Comment: Good annotation databases for a VCF file (somatic variants)
3.9 years ago by Collin ▴ 1000
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6.4k
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Comment: Comment: Good annotation databases for a VCF file (somatic variants)
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 4.1 years ago by 150k • written 4.3 years ago by ▴ 1000
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Comment: C: VEP is very slow. Fork doesnt seem to work
4.1 years ago by Collin ▴ 1000
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4.3k
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Comment: C: VEP is very slow. Fork doesnt seem to work
4.1 years ago by Collin ▴ 1000
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3.2k
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Comment: C: Is there a tool to predict if a missense variant causes a loss of function on th
4.3 years ago by Collin ▴ 1000
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27k
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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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2.5k
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Comment: C: TCGA driver mutation data
4.5 years ago by Collin ▴ 1000
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1.8k
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Comment: C: Protein_Change in MAF
4.5 years ago by Collin ▴ 1000
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2.5k
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Comment: C: TCGA driver mutation data
4.5 years ago by Collin ▴ 1000
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2.5k
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Comment: C: TCGA driver mutation data
4.5 years ago by Collin ▴ 1000
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2.5k
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Comment: C: TCGA driver mutation data
4.5 years ago by Collin ▴ 1000
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2.5k
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Comment: C: TCGA driver mutation data
4.5 years ago by Collin ▴ 1000
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2.5k
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Answer: C: TCGA driver mutation data
4.5 years ago by Collin ▴ 1000
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1.5k
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Comment: C: Variant Calling scRNA-seq data for KRAS mutations
4.6 years ago by Collin ▴ 1000
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1.5k
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Comment: C: Variant Calling scRNA-seq data for KRAS mutations
4.6 years ago by Collin ▴ 1000
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Comment: C: Get clinVar info for SNP with VEP
4.9 years ago by Collin ▴ 1000
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5.7k
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Comment: C: Get clinVar info for SNP with VEP
4.9 years ago by Collin ▴ 1000
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5.7k
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Answer: C: Get clinVar info for SNP with VEP
4.9 years ago by Collin ▴ 1000
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1.2k
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Comment: C: Variant effect prediction
5.0 years ago by Collin ▴ 1000
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1.7k
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Comment: C: How to go from VCF file to protein level
5.0 years ago by Collin ▴ 1000
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1.3k
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Comment: C: Mutation clustering in protein domains
5.1 years ago by Collin ▴ 1000
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1.8k
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Comment: C: How to download passenger mutations for cancer
5.1 years ago by Collin ▴ 1000
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1.8k
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Comment: C: How to download passenger mutations for cancer
5.1 years ago by Collin ▴ 1000
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1.8k
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Answer: A: How to download passenger mutations for cancer
5.1 years ago by Collin ▴ 1000
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6.3k
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Tool: CRAVAT: a web tool to annotate and analyze cancer variants
sequencing variant annotation Cancer
updated 3.2 years ago by 45k • written 9.5 years ago by ▴ 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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Comment: C: Can't open file 'features': [Errno 2] No such file or directory
5.2 years ago by Collin ▴ 1000
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1
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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
2
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1
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1.5k
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Answer: A: Cancer driver mutations Identification from VCFs
5.2 years ago by Collin ▴ 1000
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1.5k
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Comment: C: Suggested tool or algorithm for accessing pathogenicity and prioritization of so
5.2 years ago by Collin ▴ 1000
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1
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1.5k
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Comment: C: Suggested tool or algorithm for accessing pathogenicity and prioritization of so
5.2 years ago by Collin ▴ 1000
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3.6k
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Comment: C: Interesting things to do with 23andme data
5.2 years ago by Collin ▴ 1000
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767
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Answer: A: about snp prediction
5.2 years ago by Collin ▴ 1000
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1.4k
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Answer: A: Somatic Variant Annotation and Interpretation
5.2 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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1
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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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1
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3.0k
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Answer: A: Are there certain mutations ubiquitous in ALL cancers?
updated 5.4 years ago by 45k • written 9.4 years ago by ▴ 1000
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5.6k
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Comment: C: pathogenicity predictors of cancer mutations
5.8 years ago by Collin ▴ 1000
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5.1k
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Comment: C: Which Driver-Gene Detecting Software Supports hg38?
5.8 years ago by Collin ▴ 1000
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5.1k
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Comment: C: Which Driver-Gene Detecting Software Supports hg38?
5.8 years ago by Collin ▴ 1000
120 results • Page 1 of 3
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