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2
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3.0k
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Answer: A: How to start Gene Analysis?
9.6 years ago by Amitm ★ 2.3k
1
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0
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2.9k
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Answer: A: RNA Seq coverage
9.6 years ago by Amitm ★ 2.3k
0
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0
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1.4k
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Comment: C: Proteins types used in ENCODE
9.6 years ago by Amitm ★ 2.3k
0
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0
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2.8k
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Comment: C: Infer loss of heterozygosity from SNP variant frequencies
9.6 years ago by Amitm ★ 2.3k
0
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1
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2.2k
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Comment: C: Capillary sequencing data analysis
9.6 years ago by Amitm ★ 2.3k
0
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0
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3.3k
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Comment: C: TCGA Analysis - Generating Count files using htseq
9.6 years ago by Amitm ★ 2.3k
1
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1
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2.2k
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Answer: A: Capillary sequencing data analysis
9.6 years ago by Amitm ★ 2.3k
0
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1
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2.8k
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Answer: A: Infer loss of heterozygosity from SNP variant frequencies
9.6 years ago by Amitm ★ 2.3k
1
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0
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3.0k
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Comment: C: Assembled TCGA dataset download
9.6 years ago by Amitm ★ 2.3k
0
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0
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1.4k
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Comment: C: When assembling transcriptomes based on a reference why are the 5' and 3' UTRs c
9.6 years ago by Amitm ★ 2.3k
0
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1
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3.0k
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Answer: A: Assembled TCGA dataset download
9.6 years ago by Amitm ★ 2.3k
1
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0
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1.4k
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Answer: A: how to check which probesets belong to which transcript?
9.6 years ago by Amitm ★ 2.3k
1
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0
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8.4k
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Comment: C: Annotation of Structural Variants and CNVs
9.6 years ago by Amitm ★ 2.3k
1
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0
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2.1k
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Comment: C: Using cbioportal gene ontology for new gene/variants discovery
9.6 years ago by Amitm ★ 2.3k
0
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0
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5.8k
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Comment: C: how to understand gene fusion and how to call gene fusion ?
9.6 years ago by Amitm ★ 2.3k
0
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1
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8.8k
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Comment: C: TCGA clinical data: stage of tumor at time biopsy was taken
9.6 years ago by Amitm ★ 2.3k
0
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0
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5.8k
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Comment: C: how to understand gene fusion and how to call gene fusion ?
9.6 years ago by Amitm ★ 2.3k
2
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2
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5.8k
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Answer: A: how to understand gene fusion and how to call gene fusion ?
9.6 years ago by Amitm ★ 2.3k
1
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0
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2.5k
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Answer: A: Annotation: From GO to IPS
9.6 years ago by Amitm ★ 2.3k
0
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0
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3.2k
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Comment: C: varscan2 mpileup2snp output contains indels
9.6 years ago by Amitm ★ 2.3k
1
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1
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4.2k
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Answer: A: How to find exact allele frequency for the SNP/indel variants ?
9.6 years ago by Amitm ★ 2.3k
0
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0
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4.9k
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Comment: C: Filtering reads aligned to specific chromosome
9.7 years ago by Amitm ★ 2.3k
0
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1
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4.9k
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Comment: C: Filtering reads aligned to specific chromosome
9.7 years ago by Amitm ★ 2.3k
0
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1
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4.9k
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Answer: A: Filtering reads aligned to specific chromosome
9.7 years ago by Amitm ★ 2.3k
1
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0
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10k
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Comment: C: Variant caller for low frequency variants
9.7 years ago by Amitm ★ 2.3k
0
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0
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3.3k
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Answer: A: TCGA RNAseq normal and tumor samples problem
9.7 years ago by Amitm ★ 2.3k
1
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0
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1.7k
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Answer: A: Interreplicate statistics for microarray data?
9.7 years ago by Amitm ★ 2.3k
1
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1
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2.8k
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Comment: C: Possible to find bioinformatician postdoc if I only could use other's programs a
9.7 years ago by Amitm ★ 2.3k
4
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0
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10k
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Answer: A: Variant caller for low frequency variants
9.7 years ago by Amitm ★ 2.3k
0
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1
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5.8k
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Comment: C: issues with the precalculated lookup in Interproscan-5.17-56.0
9.7 years ago by Amitm ★ 2.3k
0
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2
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5.8k
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Answer: A: issues with the precalculated lookup in Interproscan-5.17-56.0
9.7 years ago by Amitm ★ 2.3k
1
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1
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4.0k
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Comment: C: HLA typing from NGS data (HLAreporter and HLAcaller)
9.7 years ago by Amitm ★ 2.3k
0
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1
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7.0k
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Comment: C: Download human 3 UTR FASTA file
9.7 years ago by Amitm ★ 2.3k
0
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1
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7.0k
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Comment: C: Download human 3 UTR FASTA file
9.7 years ago by Amitm ★ 2.3k
2
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1
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6.8k
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Answer: C: Machine Learning - RNAseq
9.7 years ago by Amitm ★ 2.3k
1
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0
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2.8k
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Answer: Answer: Source for Normals for Bladder Cancer RNA-Seq
updated 3.6 years ago by 45k • written 9.7 years ago by ★ 2.3k
0
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0
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2.5k
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Comment: C: Experimental method to count the mean number of DNA-bound transcription factors
9.7 years ago by Amitm ★ 2.3k
0
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1
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2.5k
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Comment: C: Experimental method to count the mean number of DNA-bound transcription factors
9.7 years ago by Amitm ★ 2.3k
1
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0
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2.0k
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Answer: Answer: Please suggest a suitable tool for GO annotation of a plant de novo assembled tr
updated 3.3 years ago by 45k • written 9.7 years ago by ★ 2.3k
0
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0
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2.0k
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Answer: A: mapping known epitopes in a protein sequcence
9.7 years ago by Amitm ★ 2.3k
3
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1
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3.8k
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Comment: C: Imprresive demonstration about bioinformatics analysis.
9.7 years ago by Amitm ★ 2.3k
0
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1
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8.1k
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Comment: C: How to calculate enrichment P-value?
9.7 years ago by Amitm ★ 2.3k
2
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1
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8.1k
views
Answer: Answer: How to calculate enrichment P-value?
updated 3.3 years ago by 45k • written 9.7 years ago by ★ 2.3k
1
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1
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4.5k
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Comment: Comment: mapping RNAseq reads to a genbank isoforme that is not in Reference Annotation
updated 3.3 years ago by 45k • written 9.7 years ago by ★ 2.3k
1
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1
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4.5k
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Comment: Comment: mapping RNAseq reads to a genbank isoforme that is not in Reference Annotation
updated 3.3 years ago by 45k • written 9.7 years ago by ★ 2.3k
0
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0
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2.2k
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Answer: Answer: Regarding Human Exon Variant Reference
updated 3.3 years ago by 45k • written 9.7 years ago by ★ 2.3k
1
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0
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2.3k
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Comment: Comment: illumina microarray gene Technology
updated 3.3 years ago by 45k • written 9.7 years ago by ★ 2.3k
0
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1
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4.1k
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Comment: C: analyzing RNAseq data in cytoscape
9.8 years ago by Amitm ★ 2.3k
1
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1
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4.9k
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Comment: C: Ensembl BioMart - How to get Transcript IDs version increment?
9.8 years ago by Amitm ★ 2.3k
1
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1
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5.2k
views
Answer: A: What's wrong with this sample? (kmers found by FastQC of RNA-Seq)
9.8 years ago by Amitm ★ 2.3k
280 results • Page 5 of 6
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