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2
votes
6
replies
1.8k
views
How to do Genome Annotation?
GenomeAnnotation
updated 2.0 years ago by ▴ 50 • written 6.3 years ago by ▴ 60
0
votes
0
replies
1.4k
views
MLST and resfinder analysis got failed
MLST ResFinder
updated 4.2 years ago by 20 • written 6.1 years ago by ▴ 60
1
vote
1
reply
3.6k
views
Primer design for HLA locus.
primer-design HLA
updated 12 months ago by 39k • written 8.2 years ago by ▴ 60
0
votes
0
replies
926
views
Hi blog any one worked on ClinSeK tool? Is it accurate ?
ClinSeK
updated 5.0 years ago by 20 • written 8.1 years ago by ▴ 60
3
votes
5
replies
2.1k
views
How to convert fastq file with raw reads to draft genome fastq file ?
fastq
updated 5.9 years ago by 20 • written 6.1 years ago by ▴ 60
13
votes
7
replies
5.9k
views
Any One please provide protocol for Analysing long noncoding RNA illumina NGS data ?
RSeQC RNA-SeQC noncodingRNA
updated 6.2 years ago by 20 • written 6.8 years ago by ▴ 60
2
votes
2
replies
2.0k
views
removing PCR duplicates from MedipSeq Data
removePCRduplicates Medipseq
updated 6.4 years ago by 9.6k • written 6.4 years ago by ▴ 60
0
votes
0
replies
1.5k
views
error while executing MeDUSA package in redhat server
MeDUSA
6.4 years ago by gskbioinfo143 ▴ 60
1
vote
1
reply
1.7k
views
Need Clarity/ Suggestions on Medip Seq Data analysis
MeDSeq
6.4 years ago by gskbioinfo143 ▴ 60
1
vote
7
replies
2.0k
views
Quality check of Medip Seq Data
Fastqc qualityanalysis MedipSeq
updated 6.4 years ago by 20 • written 6.5 years ago by ▴ 60
0
votes
3
replies
2.8k
views
DiffBind installation error in R & Rstudio?
DiffBind
updated 6.7 years ago by ★ 3.2k • written 6.7 years ago by ▴ 60
3
votes
6
replies
1.5k
views
Control data for chip-seq analysis of SRX681547, SRX681548 data
ChIP-Seq
updated 6.8 years ago by 103k • written 6.8 years ago by ▴ 60
0
votes
2
replies
1.6k
views
Where I can get HLA cellines .bam file sequenced using IonPGM ?
HLA Cell-line IontorrentPGM
updated 13 months ago by 39k • written 7.3 years ago by ▴ 60
1
vote
5
replies
3.7k
views
how to design primers for IKBKG gene if it has pseudo gene?
primerdesign
updated 7.4 years ago by 52k • written 7.4 years ago by ▴ 60
1
vote
1
reply
2.3k
views
How to get genotype data for these cell lines?
Genotype-Data cellline-data
updated 10 months ago by 39k • written 7.5 years ago by ▴ 60
0
votes
0
replies
738
views
how to get Genotype data and its frequency for Caucasian populations
Genotype data genotype frequency
7.6 years ago by gskbioinfo143 ▴ 60
0
votes
0
replies
1.6k
views
How to get HapMap Data for cell line NA10843 ?
HAPMAP
7.8 years ago by gskbioinfo143 ▴ 60
0
votes
1
reply
2.8k
views
RNA-SeQC result interpretation
RNA-SeQC RNA-Seq
updated 7 months ago by 39k • written 7.8 years ago by ▴ 60
0
votes
4
replies
4.4k
views
How to get read group information for bam file
RNA-Seq
updated 7 months ago by 39k • written 7.8 years ago by ▴ 60
3
votes
6
replies
2.6k
views
Where to get chromosome start end positions for this COSMIC IDs?
Cosmic
updated 7 months ago by 39k • written 7.8 years ago by ▴ 60
0
votes
0
replies
1.4k
views
which database to prefer for creating NGS Disease related Panels?
NGS Panel COSMIC TCGA ICGC
7.8 years ago by gskbioinfo143 ▴ 60
3
votes
3
replies
2.4k
views
How to find out off target reads?
iontorrent RNA-Seq Off-Target-Reads
updated 6 months ago by 39k • written 7.9 years ago by ▴ 60
2
votes
4
replies
1.8k
views
How to get DEPTH, as well as variant calling of transcriptome data
RNA-Seq
updated 5 months ago by 39k • written 7.9 years ago by ▴ 60
2
votes
2
replies
1.2k
views
tool or software to design graphical images for given fusion gene data?
tool
8.0 years ago by gskbioinfo143 ▴ 60
7
votes
4
replies
3.3k
views
Hi blog how to calculate differntial expression analysis if thre is no replicates in count data using edgeR?
edgeR
updated 4 months ago by 39k • written 8.0 years ago by ▴ 60
3
votes
1
reply
2.1k
views
Hey any one used QC-Chain tool?
QC-Chain
updated 8.0 years ago by 34k • written 8.0 years ago by ▴ 60
1
vote
1
reply
1.3k
views
How to find out binned matched reads with in particular chr region?
coverage matched reads binned
updated 8.1 years ago by 20 • written 8.1 years ago by ▴ 60
4
votes
9
replies
5.7k
views
Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only chr21?
coverage bedtools
updated 10 months ago by 39k • written 8.1 years ago by ▴ 60
0
votes
3
replies
2.9k
views
Tool to detect Copy Number Variations(CNV) using Single Read End Data
CNV
updated 11 months ago by 39k • written 8.1 years ago by ▴ 60
0
votes
4
replies
922
views
Tool to check Number of cells covered in the RNA sample after RNA-Seq analysis?
RNA-Seq
updated 11 months ago by 39k • written 8.1 years ago by ▴ 60
2
votes
2
replies
1.4k
views
how to identify mutations transmitted from parents to child?
mutation
8.2 years ago by gskbioinfo143 ▴ 60
0
votes
1
reply
2.6k
views
Is there any pipeline for CNV Detection of NGS Data other than Ion Reporter?
CNV NGS Pipeline
updated 8.2 years ago by 7.4k • written 8.2 years ago by ▴ 60
8
votes
5
replies
2.2k
views
whre we can get BRCA1 and 2 SNPs data for indian population?
SNP BRCA2 indian-population BRCA1
updated 12 months ago by 39k • written 8.2 years ago by ▴ 60
0
votes
1
reply
1.6k
views
Hey what is the accurate procedure for insilico-primer design for STR loci?
STR Loci Insilico primerdesign CODIS
updated 12 months ago by 39k • written 8.2 years ago by ▴ 60
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