Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : comments
0
votes
1
reply
2.0k
views
Comment: C: Capillary sequencing data analysis
9.2 years ago by Amitm ★ 2.3k
0
votes
0
replies
3.2k
views
Comment: C: TCGA Analysis - Generating Count files using htseq
9.2 years ago by Amitm ★ 2.3k
1
vote
0
replies
2.9k
views
Comment: C: Assembled TCGA dataset download
9.2 years ago by Amitm ★ 2.3k
0
votes
0
replies
1.3k
views
Comment: C: When assembling transcriptomes based on a reference why are the 5' and 3' UTRs c
9.2 years ago by Amitm ★ 2.3k
1
vote
0
replies
7.9k
views
Comment: C: Annotation of Structural Variants and CNVs
9.3 years ago by Amitm ★ 2.3k
1
vote
0
replies
2.1k
views
Comment: C: Using cbioportal gene ontology for new gene/variants discovery
9.3 years ago by Amitm ★ 2.3k
0
votes
0
replies
5.5k
views
Comment: C: how to understand gene fusion and how to call gene fusion ?
9.3 years ago by Amitm ★ 2.3k
0
votes
1
reply
8.0k
views
Comment: C: TCGA clinical data: stage of tumor at time biopsy was taken
9.3 years ago by Amitm ★ 2.3k
0
votes
0
replies
5.5k
views
Comment: C: how to understand gene fusion and how to call gene fusion ?
9.3 years ago by Amitm ★ 2.3k
0
votes
0
replies
3.1k
views
Comment: C: varscan2 mpileup2snp output contains indels
9.3 years ago by Amitm ★ 2.3k
0
votes
0
replies
4.5k
views
Comment: C: Filtering reads aligned to specific chromosome
9.3 years ago by Amitm ★ 2.3k
0
votes
1
reply
4.5k
views
Comment: C: Filtering reads aligned to specific chromosome
9.3 years ago by Amitm ★ 2.3k
1
vote
0
replies
9.2k
views
Comment: C: Variant caller for low frequency variants
9.3 years ago by Amitm ★ 2.3k
1
vote
1
reply
2.6k
views
Comment: C: Possible to find bioinformatician postdoc if I only could use other's programs a
9.3 years ago by Amitm ★ 2.3k
0
votes
1
reply
5.5k
views
Comment: C: issues with the precalculated lookup in Interproscan-5.17-56.0
9.3 years ago by Amitm ★ 2.3k
1
vote
1
reply
3.8k
views
Comment: C: HLA typing from NGS data (HLAreporter and HLAcaller)
9.3 years ago by Amitm ★ 2.3k
0
votes
1
reply
6.7k
views
Comment: C: Download human 3 UTR FASTA file
9.3 years ago by Amitm ★ 2.3k
0
votes
1
reply
6.7k
views
Comment: C: Download human 3 UTR FASTA file
9.3 years ago by Amitm ★ 2.3k
0
votes
0
replies
2.3k
views
Comment: C: Experimental method to count the mean number of DNA-bound transcription factors
9.3 years ago by Amitm ★ 2.3k
0
votes
1
reply
2.3k
views
Comment: C: Experimental method to count the mean number of DNA-bound transcription factors
9.3 years ago by Amitm ★ 2.3k
3
votes
1
reply
3.4k
views
Comment: C: Imprresive demonstration about bioinformatics analysis.
9.3 years ago by Amitm ★ 2.3k
0
votes
1
reply
7.9k
views
Comment: C: How to calculate enrichment P-value?
9.3 years ago by Amitm ★ 2.3k
1
vote
1
reply
4.0k
views
Comment: Comment: mapping RNAseq reads to a genbank isoforme that is not in Reference Annotation
updated 2.9 years ago by 45k • written 9.3 years ago by ★ 2.3k
1
vote
1
reply
4.0k
views
Comment: Comment: mapping RNAseq reads to a genbank isoforme that is not in Reference Annotation
updated 2.9 years ago by 45k • written 9.3 years ago by ★ 2.3k
1
vote
0
replies
2.1k
views
Comment: Comment: illumina microarray gene Technology
updated 2.9 years ago by 45k • written 9.3 years ago by ★ 2.3k
0
votes
1
reply
3.7k
views
Comment: C: analyzing RNAseq data in cytoscape
9.4 years ago by Amitm ★ 2.3k
1
vote
1
reply
4.4k
views
Comment: C: Ensembl BioMart - How to get Transcript IDs version increment?
9.4 years ago by Amitm ★ 2.3k
0
votes
1
reply
3.7k
views
Comment: C: analyzing RNAseq data in cytoscape
9.4 years ago by Amitm ★ 2.3k
1
vote
0
replies
4.6k
views
Comment: C: Reference and dbSNP incompatibility issue (MuTect2)
9.4 years ago by Amitm ★ 2.3k
0
votes
1
reply
1.2k
views
Comment: C: RNAseq large differences in mapping
9.4 years ago by Amitm ★ 2.3k
1
vote
0
replies
6.3k
views
Comment: C: Something better than GSEA?
9.4 years ago by Amitm ★ 2.3k
0
votes
0
replies
5.9k
views
Comment: C: alignment rate in bowtie2
9.4 years ago by Amitm ★ 2.3k
1
vote
1
reply
5.9k
views
Comment: C: alignment rate in bowtie2
9.4 years ago by Amitm ★ 2.3k
0
votes
0
replies
2.5k
views
Comment: C: Which tool for pathway analysis ?
9.4 years ago by Amitm ★ 2.3k
0
votes
0
replies
8.8k
views
Comment: C: RefSeq Ids(NM*, NR*) to ensemble transcript Ids (ENST*)
9.4 years ago by Amitm ★ 2.3k
0
votes
0
replies
2.2k
views
Comment: C: What NGS courses would you like us to prepare for 2016? (one week left)
9.4 years ago by Amitm ★ 2.3k
1
vote
0
replies
2.8k
views
Comment: C: RNA-Seq quantitation for human, paired end vs single end, strand specific or not
9.4 years ago by Amitm ★ 2.3k
0
votes
1
reply
4.4k
views
Comment: C: Somatic allele frequency from TCGA in non-coding DNA
9.4 years ago by Amitm ★ 2.3k
1
vote
1
reply
4.4k
views
Comment: C: Somatic allele frequency from TCGA in non-coding DNA
9.4 years ago by Amitm ★ 2.3k
0
votes
0
replies
2.8k
views
Comment: C: Rna-Seq alternative splicing analysis under limited conditions: possible?
9.4 years ago by Amitm ★ 2.3k
0
votes
0
replies
27k
views
Comment: C: Kmer Content in FastQC failed
9.4 years ago by Amitm ★ 2.3k
1
vote
1
reply
6.6k
views
Comment: C: How to decide the quality of RNA-seq analysis
9.4 years ago by Amitm ★ 2.3k
0
votes
1
reply
4.0k
views
Comment: C: Removing PCR primers in targeted sequencing with nested amplicons
9.4 years ago by Amitm ★ 2.3k
0
votes
1
reply
4.0k
views
Comment: C: Removing PCR primers in targeted sequencing with nested amplicons
9.4 years ago by Amitm ★ 2.3k
0
votes
0
replies
5.5k
views
Comment: C: How to calculate read depth and coverage for whole exome sequencing?
9.4 years ago by Amitm ★ 2.3k
4
votes
1
reply
2.7k
views
Comment: C: Assemble fully overlapping reads into contigs that may have several clones
9.4 years ago by Amitm ★ 2.3k
0
votes
0
replies
2.7k
views
Comment: C: checking many somatic mutations in IGV
9.4 years ago by Amitm ★ 2.3k
197 results • Page 4 of 4
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6