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Comment: C: How to search for consensus sequence in RNA-seq data?
7.3 years ago by Samuel Brady ▴ 330
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Answer: A: cBioportal survival analysis help
7.3 years ago by Samuel Brady ▴ 330
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Comment: C: mutation signatures from MAF's, and decompose them into Stratton signatures
7.3 years ago by Samuel Brady ▴ 330
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Answer: A: ROC for biomarker discovery
7.3 years ago by Samuel Brady ▴ 330
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Answer: A: How to find RNASeq V2 RSEM normalized expression values for various cancer studi
7.3 years ago by Samuel Brady ▴ 330
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Comment: C: From sam data, how do I tell from which fastq file each read came from?
7.3 years ago by Samuel Brady ▴ 330
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3.7k
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Answer: A: Are there downloadable DBs for hotspot mutations?
7.3 years ago by Samuel Brady ▴ 330
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Answer: A: Is SNPeff still the standard for variant effect prediction?
7.3 years ago by Samuel Brady ▴ 330
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Answer: A: multi-omics data gene set enrichment analysis
7.4 years ago by Samuel Brady ▴ 330
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1.9k
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Answer: Answer: Intronic Variant Filtering
updated 8 months ago by 44k • written 7.4 years ago by ▴ 330
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Comment: C: how to find a read by name in a bam file
7.4 years ago by Samuel Brady ▴ 330
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10k
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Comment: A: how to find a read by name in a bam file
7.4 years ago by Samuel Brady ▴ 330
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Answer: A: What is the unit of RNASeq v2 mRNA expression profile in cross-cancer query?
7.4 years ago by Samuel Brady ▴ 330
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Comment: C: Returning gene functional annotations with gene symbols as input (using mygene B
7.4 years ago by Samuel Brady ▴ 330
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3.8k
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Comment: C: General questions about running GSEAPreranked
7.4 years ago by Samuel Brady ▴ 330
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3.0k
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Answer: A: Returning gene functional annotations with gene symbols as input (using mygene B
7.4 years ago by Samuel Brady ▴ 330
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3.2k
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Answer: A: how to calling variants in RNAseq data from multiple samples?
7.4 years ago by Samuel Brady ▴ 330
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Comment: C: How to account for cell type composition in differential expression analysis?
7.4 years ago by Samuel Brady ▴ 330
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3.8k
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Answer: A: General questions about running GSEAPreranked
7.4 years ago by Samuel Brady ▴ 330
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Answer: A: What Computational Tools Specialize in Human Cell Types?
7.4 years ago by Samuel Brady ▴ 330
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Answer: A: Metagenomic Mappers & Benchmark Datasets?
7.4 years ago by Samuel Brady ▴ 330
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1.7k
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Answer: A: Group mutations in SNP data
7.4 years ago by Samuel Brady ▴ 330
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2.6k
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Comment: C: Samtools mpileup degenerative characters
7.4 years ago by Samuel Brady ▴ 330
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3.0k
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Comment: C: How to account for cell type composition in differential expression analysis?
7.4 years ago by Samuel Brady ▴ 330
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1.1k
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Answer: A: Retrieving identical positions from mpileup file
7.4 years ago by Samuel Brady ▴ 330
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1.5k
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Answer: A: Map from GEO samples' name to TCGA name
7.4 years ago by Samuel Brady ▴ 330
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1
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1.7k
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Answer: A: Get mRNA, miRNA, lncRNA specific for probes
7.4 years ago by Samuel Brady ▴ 330
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3.8k
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Answer: A: sciClone + clonEvol on WES
7.4 years ago by Samuel Brady ▴ 330
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3.0k
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Answer: A: How to account for cell type composition in differential expression analysis?
7.4 years ago by Samuel Brady ▴ 330
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6.0k
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Answer: A: problem with chromosomes in michigan imputation server
7.4 years ago by Samuel Brady ▴ 330
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14k
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Answer: A: Heatmap.2 giving specific color to a value and start gradient after
7.4 years ago by Samuel Brady ▴ 330
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1
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4.3k
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Answer: A: converting very small p-values into chi-squared statistics with python
7.4 years ago by Samuel Brady ▴ 330
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2.6k
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Answer: A: Publicly-available disease genome VCF
7.4 years ago by Samuel Brady ▴ 330
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14k
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Comment: C: GSVA analysis in R: How to use my geneset and expression data matrix in GSVA.
7.4 years ago by Samuel Brady ▴ 330
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1.7k
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Answer: A: how to do gene annotation
7.4 years ago by Samuel Brady ▴ 330
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17k
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Answer: A: Trouble installing R package Cairo
7.4 years ago by Samuel Brady ▴ 330
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2.3k
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Answer: A: Advice needed on RNAseq technical and biological replicates analysis using DEseq
7.4 years ago by Samuel Brady ▴ 330
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2.2k
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Answer: A: Question about best way to extraction mates of reads
7.5 years ago by Samuel Brady ▴ 330
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3.1k
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Comment: C: Are there NGS-based CNV callers that utilise allele frequency?
7.5 years ago by Samuel Brady ▴ 330
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1.6k
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Answer: A: Cancer database with both germline and genome-wide sequencing data
7.5 years ago by Samuel Brady ▴ 330
2
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1
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3.1k
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Answer: A: Are there NGS-based CNV callers that utilise allele frequency?
7.5 years ago by Samuel Brady ▴ 330
41 results • Page 1 of 1
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