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0
votes
1
reply
1.9k
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Comment:
C: Capillary sequencing data analysis
8.6 years ago by
Amitm
★ 2.3k
0
votes
0
replies
3.0k
views
Comment:
C: TCGA Analysis - Generating Count files using htseq
8.6 years ago by
Amitm
★ 2.3k
1
vote
0
replies
2.7k
views
Comment:
C: Assembled TCGA dataset download
8.6 years ago by
Amitm
★ 2.3k
0
votes
0
replies
1.2k
views
Comment:
C: When assembling transcriptomes based on a reference why are the 5' and 3' UTRs c
8.6 years ago by
Amitm
★ 2.3k
1
vote
0
replies
7.1k
views
Comment:
C: Annotation of Structural Variants and CNVs
8.6 years ago by
Amitm
★ 2.3k
1
vote
0
replies
1.9k
views
Comment:
C: Using cbioportal gene ontology for new gene/variants discovery
8.6 years ago by
Amitm
★ 2.3k
0
votes
0
replies
5.2k
views
Comment:
C: how to understand gene fusion and how to call gene fusion ?
8.6 years ago by
Amitm
★ 2.3k
0
votes
1
reply
7.1k
views
Comment:
C: TCGA clinical data: stage of tumor at time biopsy was taken
8.6 years ago by
Amitm
★ 2.3k
0
votes
0
replies
5.2k
views
Comment:
C: how to understand gene fusion and how to call gene fusion ?
8.6 years ago by
Amitm
★ 2.3k
0
votes
0
replies
3.0k
views
Comment:
C: varscan2 mpileup2snp output contains indels
8.7 years ago by
Amitm
★ 2.3k
0
votes
0
replies
4.0k
views
Comment:
C: Filtering reads aligned to specific chromosome
8.7 years ago by
Amitm
★ 2.3k
0
votes
1
reply
4.0k
views
Comment:
C: Filtering reads aligned to specific chromosome
8.7 years ago by
Amitm
★ 2.3k
1
vote
0
replies
8.3k
views
Comment:
C: Variant caller for low frequency variants
8.7 years ago by
Amitm
★ 2.3k
1
vote
1
reply
2.3k
views
Comment:
C: Possible to find bioinformatician postdoc if I only could use other's programs a
8.7 years ago by
Amitm
★ 2.3k
0
votes
1
reply
5.2k
views
Comment:
C: issues with the precalculated lookup in Interproscan-5.17-56.0
8.7 years ago by
Amitm
★ 2.3k
1
vote
1
reply
3.7k
views
Comment:
C: HLA typing from NGS data (HLAreporter and HLAcaller)
8.7 years ago by
Amitm
★ 2.3k
0
votes
1
reply
6.3k
views
Comment:
C: Download human 3 UTR FASTA file
8.7 years ago by
Amitm
★ 2.3k
0
votes
1
reply
6.3k
views
Comment:
C: Download human 3 UTR FASTA file
8.7 years ago by
Amitm
★ 2.3k
0
votes
0
replies
2.1k
views
Comment:
C: Experimental method to count the mean number of DNA-bound transcription factors
8.7 years ago by
Amitm
★ 2.3k
0
votes
1
reply
2.1k
views
Comment:
C: Experimental method to count the mean number of DNA-bound transcription factors
8.7 years ago by
Amitm
★ 2.3k
3
votes
1
reply
3.0k
views
Comment:
C: Imprresive demonstration about bioinformatics analysis.
8.7 years ago by
Amitm
★ 2.3k
0
votes
1
reply
7.6k
views
Comment:
C: How to calculate enrichment P-value?
8.7 years ago by
Amitm
★ 2.3k
1
vote
1
reply
3.5k
views
Comment:
Comment: mapping RNAseq reads to a genbank isoforme that is not in Reference Annotation
updated 2.3 years ago by
Ram
44k • written 8.7 years ago by
Amitm
★ 2.3k
1
vote
1
reply
3.5k
views
Comment:
Comment: mapping RNAseq reads to a genbank isoforme that is not in Reference Annotation
updated 2.3 years ago by
Ram
44k • written 8.7 years ago by
Amitm
★ 2.3k
1
vote
0
replies
1.9k
views
Comment:
Comment: illumina microarray gene Technology
updated 2.3 years ago by
Ram
44k • written 8.7 years ago by
Amitm
★ 2.3k
0
votes
1
reply
3.1k
views
Comment:
C: analyzing RNAseq data in cytoscape
8.8 years ago by
Amitm
★ 2.3k
1
vote
1
reply
3.6k
views
Comment:
C: Ensembl BioMart - How to get Transcript IDs version increment?
8.8 years ago by
Amitm
★ 2.3k
0
votes
1
reply
3.1k
views
Comment:
C: analyzing RNAseq data in cytoscape
8.8 years ago by
Amitm
★ 2.3k
1
vote
0
replies
4.2k
views
Comment:
C: Reference and dbSNP incompatibility issue (MuTect2)
8.8 years ago by
Amitm
★ 2.3k
0
votes
1
reply
1.1k
views
Comment:
C: RNAseq large differences in mapping
8.8 years ago by
Amitm
★ 2.3k
1
vote
0
replies
5.5k
views
Comment:
C: Something better than GSEA?
8.8 years ago by
Amitm
★ 2.3k
0
votes
0
replies
5.4k
views
Comment:
C: alignment rate in bowtie2
8.8 years ago by
Amitm
★ 2.3k
1
vote
1
reply
5.4k
views
Comment:
C: alignment rate in bowtie2
8.8 years ago by
Amitm
★ 2.3k
0
votes
0
replies
2.3k
views
Comment:
C: Which tool for pathway analysis ?
8.8 years ago by
Amitm
★ 2.3k
0
votes
0
replies
8.2k
views
Comment:
C: RefSeq Ids(NM*, NR*) to ensemble transcript Ids (ENST*)
8.8 years ago by
Amitm
★ 2.3k
0
votes
0
replies
2.0k
views
Comment:
C: What NGS courses would you like us to prepare for 2016? (one week left)
8.8 years ago by
Amitm
★ 2.3k
1
vote
0
replies
2.7k
views
Comment:
C: RNA-Seq quantitation for human, paired end vs single end, strand specific or not
8.8 years ago by
Amitm
★ 2.3k
0
votes
1
reply
3.7k
views
Comment:
C: Somatic allele frequency from TCGA in non-coding DNA
8.8 years ago by
Amitm
★ 2.3k
1
vote
1
reply
3.7k
views
Comment:
C: Somatic allele frequency from TCGA in non-coding DNA
8.8 years ago by
Amitm
★ 2.3k
0
votes
0
replies
2.3k
views
Comment:
C: Rna-Seq alternative splicing analysis under limited conditions: possible?
8.8 years ago by
Amitm
★ 2.3k
0
votes
0
replies
26k
views
Comment:
C: Kmer Content in FastQC failed
8.8 years ago by
Amitm
★ 2.3k
1
vote
1
reply
5.7k
views
Comment:
C: How to decide the quality of RNA-seq analysis
8.8 years ago by
Amitm
★ 2.3k
0
votes
1
reply
3.7k
views
Comment:
C: Removing PCR primers in targeted sequencing with nested amplicons
8.8 years ago by
Amitm
★ 2.3k
0
votes
1
reply
3.7k
views
Comment:
C: Removing PCR primers in targeted sequencing with nested amplicons
8.8 years ago by
Amitm
★ 2.3k
0
votes
0
replies
5.3k
views
Comment:
C: How to calculate read depth and coverage for whole exome sequencing?
8.8 years ago by
Amitm
★ 2.3k
4
votes
1
reply
2.5k
views
Comment:
C: Assemble fully overlapping reads into contigs that may have several clones
8.8 years ago by
Amitm
★ 2.3k
0
votes
0
replies
2.5k
views
Comment:
C: checking many somatic mutations in IGV
8.8 years ago by
Amitm
★ 2.3k
197 results • Page
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