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2
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2.5k
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Answer: A: How to start Gene Analysis?
8.6 years ago by Amitm ★ 2.3k
1
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0
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2.5k
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Answer: A: RNA Seq coverage
8.6 years ago by Amitm ★ 2.3k
0
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0
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1.2k
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Comment: C: Proteins types used in ENCODE
8.6 years ago by Amitm ★ 2.3k
0
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0
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2.4k
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Comment: C: Infer loss of heterozygosity from SNP variant frequencies
8.6 years ago by Amitm ★ 2.3k
0
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1
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1.9k
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Comment: C: Capillary sequencing data analysis
8.6 years ago by Amitm ★ 2.3k
0
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0
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3.0k
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Comment: C: TCGA Analysis - Generating Count files using htseq
8.6 years ago by Amitm ★ 2.3k
1
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1
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1.9k
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Answer: A: Capillary sequencing data analysis
8.6 years ago by Amitm ★ 2.3k
0
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1
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2.4k
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Answer: A: Infer loss of heterozygosity from SNP variant frequencies
8.6 years ago by Amitm ★ 2.3k
1
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0
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2.7k
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Comment: C: Assembled TCGA dataset download
8.7 years ago by Amitm ★ 2.3k
0
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0
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1.2k
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Comment: C: When assembling transcriptomes based on a reference why are the 5' and 3' UTRs c
8.7 years ago by Amitm ★ 2.3k
0
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1
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2.7k
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Answer: A: Assembled TCGA dataset download
8.7 years ago by Amitm ★ 2.3k
1
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0
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1.2k
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Answer: A: how to check which probesets belong to which transcript?
8.7 years ago by Amitm ★ 2.3k
1
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0
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7.1k
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Comment: C: Annotation of Structural Variants and CNVs
8.7 years ago by Amitm ★ 2.3k
1
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0
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1.9k
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Comment: C: Using cbioportal gene ontology for new gene/variants discovery
8.7 years ago by Amitm ★ 2.3k
0
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0
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5.2k
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Comment: C: how to understand gene fusion and how to call gene fusion ?
8.7 years ago by Amitm ★ 2.3k
0
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1
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7.1k
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Comment: C: TCGA clinical data: stage of tumor at time biopsy was taken
8.7 years ago by Amitm ★ 2.3k
0
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0
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5.2k
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Comment: C: how to understand gene fusion and how to call gene fusion ?
8.7 years ago by Amitm ★ 2.3k
2
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2
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5.2k
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Answer: A: how to understand gene fusion and how to call gene fusion ?
8.7 years ago by Amitm ★ 2.3k
1
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0
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2.2k
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Answer: A: Annotation: From GO to IPS
8.7 years ago by Amitm ★ 2.3k
0
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0
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3.0k
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Comment: C: varscan2 mpileup2snp output contains indels
8.7 years ago by Amitm ★ 2.3k
1
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1
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3.8k
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Answer: A: How to find exact allele frequency for the SNP/indel variants ?
8.7 years ago by Amitm ★ 2.3k
0
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0
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4.0k
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Comment: C: Filtering reads aligned to specific chromosome
8.7 years ago by Amitm ★ 2.3k
0
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1
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4.0k
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Comment: C: Filtering reads aligned to specific chromosome
8.7 years ago by Amitm ★ 2.3k
0
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1
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4.0k
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Answer: A: Filtering reads aligned to specific chromosome
8.7 years ago by Amitm ★ 2.3k
1
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0
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8.3k
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Comment: C: Variant caller for low frequency variants
8.7 years ago by Amitm ★ 2.3k
0
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0
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3.1k
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Answer: A: TCGA RNAseq normal and tumor samples problem
8.7 years ago by Amitm ★ 2.3k
1
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0
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1.5k
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Answer: A: Interreplicate statistics for microarray data?
8.7 years ago by Amitm ★ 2.3k
1
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1
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2.3k
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Comment: C: Possible to find bioinformatician postdoc if I only could use other's programs a
8.7 years ago by Amitm ★ 2.3k
4
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0
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8.3k
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Answer: A: Variant caller for low frequency variants
8.7 years ago by Amitm ★ 2.3k
0
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1
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5.2k
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Comment: C: issues with the precalculated lookup in Interproscan-5.17-56.0
8.7 years ago by Amitm ★ 2.3k
0
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2
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5.2k
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Answer: A: issues with the precalculated lookup in Interproscan-5.17-56.0
8.7 years ago by Amitm ★ 2.3k
1
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1
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3.7k
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Comment: C: HLA typing from NGS data (HLAreporter and HLAcaller)
8.7 years ago by Amitm ★ 2.3k
0
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1
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6.3k
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Comment: C: Download human 3 UTR FASTA file
8.7 years ago by Amitm ★ 2.3k
0
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1
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6.3k
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Comment: C: Download human 3 UTR FASTA file
8.7 years ago by Amitm ★ 2.3k
2
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1
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5.9k
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Answer: C: Machine Learning - RNAseq
8.8 years ago by Amitm ★ 2.3k
1
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0
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2.5k
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Answer: Answer: Source for Normals for Bladder Cancer RNA-Seq
updated 2.7 years ago by 44k • written 8.8 years ago by ★ 2.3k
0
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0
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2.2k
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Comment: C: Experimental method to count the mean number of DNA-bound transcription factors
8.8 years ago by Amitm ★ 2.3k
0
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1
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2.2k
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Comment: C: Experimental method to count the mean number of DNA-bound transcription factors
8.8 years ago by Amitm ★ 2.3k
1
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0
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1.8k
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Answer: Answer: Please suggest a suitable tool for GO annotation of a plant de novo assembled tr
updated 2.4 years ago by 44k • written 8.8 years ago by ★ 2.3k
0
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0
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1.8k
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Answer: A: mapping known epitopes in a protein sequcence
8.8 years ago by Amitm ★ 2.3k
3
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1
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3.1k
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Comment: C: Imprresive demonstration about bioinformatics analysis.
8.8 years ago by Amitm ★ 2.3k
0
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1
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7.6k
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Comment: C: How to calculate enrichment P-value?
8.8 years ago by Amitm ★ 2.3k
2
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1
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7.6k
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Answer: Answer: How to calculate enrichment P-value?
updated 2.4 years ago by 44k • written 8.8 years ago by ★ 2.3k
1
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1
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3.5k
views
Comment: Comment: mapping RNAseq reads to a genbank isoforme that is not in Reference Annotation
updated 2.4 years ago by 44k • written 8.8 years ago by ★ 2.3k
1
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1
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3.5k
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Comment: Comment: mapping RNAseq reads to a genbank isoforme that is not in Reference Annotation
updated 2.4 years ago by 44k • written 8.8 years ago by ★ 2.3k
0
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0
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1.8k
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Answer: Answer: Regarding Human Exon Variant Reference
updated 2.4 years ago by 44k • written 8.8 years ago by ★ 2.3k
1
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0
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1.9k
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Comment: Comment: illumina microarray gene Technology
updated 2.4 years ago by 44k • written 8.8 years ago by ★ 2.3k
0
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1
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3.2k
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Comment: C: analyzing RNAseq data in cytoscape
8.8 years ago by Amitm ★ 2.3k
1
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1
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3.7k
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Comment: C: Ensembl BioMart - How to get Transcript IDs version increment?
8.8 years ago by Amitm ★ 2.3k
1
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1
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4.7k
views
Answer: A: What's wrong with this sample? (kmers found by FastQC of RNA-Seq)
8.8 years ago by Amitm ★ 2.3k
280 results • Page 5 of 6
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