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Comment: C: Capillary sequencing data analysis
8.5 years ago by Amitm ★ 2.3k
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2.9k
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Comment: C: TCGA Analysis - Generating Count files using htseq
8.5 years ago by Amitm ★ 2.3k
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2.7k
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Comment: C: Assembled TCGA dataset download
8.5 years ago by Amitm ★ 2.3k
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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
8.5 years ago by Amitm ★ 2.3k
1
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7.0k
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Comment: C: Annotation of Structural Variants and CNVs
8.6 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
8.6 years ago by Amitm ★ 2.3k
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0
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5.1k
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Comment: C: how to understand gene fusion and how to call gene fusion ?
8.6 years ago by Amitm ★ 2.3k
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1
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7.0k
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Comment: C: TCGA clinical data: stage of tumor at time biopsy was taken
8.6 years ago by Amitm ★ 2.3k
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0
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5.1k
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Comment: C: how to understand gene fusion and how to call gene fusion ?
8.6 years ago by Amitm ★ 2.3k
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3.0k
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Comment: C: varscan2 mpileup2snp output contains indels
8.6 years ago by Amitm ★ 2.3k
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0
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4.0k
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Comment: C: Filtering reads aligned to specific chromosome
8.6 years ago by Amitm ★ 2.3k
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1
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4.0k
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Comment: C: Filtering reads aligned to specific chromosome
8.6 years ago by Amitm ★ 2.3k
1
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0
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8.2k
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Comment: C: Variant caller for low frequency variants
8.6 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
8.6 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
8.6 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)
8.6 years ago by Amitm ★ 2.3k
0
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1
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6.2k
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Comment: C: Download human 3 UTR FASTA file
8.6 years ago by Amitm ★ 2.3k
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1
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6.2k
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Comment: C: Download human 3 UTR FASTA file
8.6 years ago by Amitm ★ 2.3k
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0
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2.1k
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Comment: C: Experimental method to count the mean number of DNA-bound transcription factors
8.7 years ago by Amitm ★ 2.3k
0
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1
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2.1k
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Comment: C: Experimental method to count the mean number of DNA-bound transcription factors
8.7 years ago by Amitm ★ 2.3k
3
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1
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3.0k
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Comment: C: Imprresive demonstration about bioinformatics analysis.
8.7 years ago by Amitm ★ 2.3k
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1
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7.6k
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Comment: C: How to calculate enrichment P-value?
8.7 years ago by Amitm ★ 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 2.2 years ago by 44k • written 8.7 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 2.2 years ago by 44k • written 8.7 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 2.2 years ago by 44k • written 8.7 years ago by ★ 2.3k
0
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1
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3.1k
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Comment: C: analyzing RNAseq data in cytoscape
8.7 years ago by Amitm ★ 2.3k
1
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1
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3.6k
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Comment: C: Ensembl BioMart - How to get Transcript IDs version increment?
8.7 years ago by Amitm ★ 2.3k
0
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1
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3.1k
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Comment: C: analyzing RNAseq data in cytoscape
8.7 years ago by Amitm ★ 2.3k
1
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0
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4.1k
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Comment: C: Reference and dbSNP incompatibility issue (MuTect2)
8.7 years ago by Amitm ★ 2.3k
0
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1
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1.0k
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Comment: C: RNAseq large differences in mapping
8.7 years ago by Amitm ★ 2.3k
1
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0
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5.4k
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Comment: C: Something better than GSEA?
8.7 years ago by Amitm ★ 2.3k
0
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0
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5.3k
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Comment: C: alignment rate in bowtie2
8.7 years ago by Amitm ★ 2.3k
1
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1
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5.3k
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Comment: C: alignment rate in bowtie2
8.7 years ago by Amitm ★ 2.3k
0
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0
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2.3k
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Comment: C: Which tool for pathway analysis ?
8.7 years ago by Amitm ★ 2.3k
0
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0
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8.2k
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Comment: C: RefSeq Ids(NM*, NR*) to ensemble transcript Ids (ENST*)
8.7 years ago by Amitm ★ 2.3k
0
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0
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2.0k
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Comment: C: What NGS courses would you like us to prepare for 2016? (one week left)
8.7 years ago by Amitm ★ 2.3k
1
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0
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2.7k
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Comment: C: RNA-Seq quantitation for human, paired end vs single end, strand specific or not
8.7 years ago by Amitm ★ 2.3k
0
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1
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3.7k
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Comment: C: Somatic allele frequency from TCGA in non-coding DNA
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: Somatic allele frequency from TCGA in non-coding DNA
8.7 years ago by Amitm ★ 2.3k
0
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0
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2.3k
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Comment: C: Rna-Seq alternative splicing analysis under limited conditions: possible?
8.7 years ago by Amitm ★ 2.3k
0
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0
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26k
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Comment: C: Kmer Content in FastQC failed
8.7 years ago by Amitm ★ 2.3k
1
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1
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5.6k
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Comment: C: How to decide the quality of RNA-seq analysis
8.8 years ago by Amitm ★ 2.3k
0
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1
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3.7k
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Comment: C: Removing PCR primers in targeted sequencing with nested amplicons
8.8 years ago by Amitm ★ 2.3k
0
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1
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3.7k
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Comment: C: Removing PCR primers in targeted sequencing with nested amplicons
8.8 years ago by Amitm ★ 2.3k
0
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0
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5.3k
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Comment: C: How to calculate read depth and coverage for whole exome sequencing?
8.8 years ago by Amitm ★ 2.3k
4
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1
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2.5k
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Comment: C: Assemble fully overlapping reads into contigs that may have several clones
8.8 years ago by Amitm ★ 2.3k
0
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0
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2.5k
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Comment: C: checking many somatic mutations in IGV
8.8 years ago by Amitm ★ 2.3k
197 results • Page 4 of 4
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