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Comment: C: how to design primers for IKBKG gene if it has pseudo gene?
updated 2.6 years ago by 36k • written 6.6 years ago by ▴ 60
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Comment: C: how to design primers for IKBKG gene if it has pseudo gene?
updated 2.6 years ago by 36k • written 6.6 years ago by ▴ 60
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Comment: C: Where to get chromosome start end positions for this COSMIC IDs?
updated 2.8 years ago by 36k • written 7.0 years ago by ▴ 60
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Comment: C: Where to get chromosome start end positions for this COSMIC IDs?
updated 2.8 years ago by 36k • written 7.0 years ago by ▴ 60
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Comment: C: How to convert fastq file with raw reads to draft genome fastq file ?
5.3 years ago by gskbioinfo143 ▴ 60
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Comment: C: How to convert fastq file with raw reads to draft genome fastq file ?
5.3 years ago by gskbioinfo143 ▴ 60
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Comment: C: How to do Genome Annotation?
5.4 years ago by gskbioinfo143 ▴ 60
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Comment: C: peakannotation by peakAnalyzer
5.6 years ago by gskbioinfo143 ▴ 60
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Comment: C: Quality check of Medip Seq Data
5.7 years ago by gskbioinfo143 ▴ 60
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1.7k
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Comment: C: Quality check of Medip Seq Data
5.7 years ago by gskbioinfo143 ▴ 60
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1.7k
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Comment: C: Quality check of Medip Seq Data
5.7 years ago by gskbioinfo143 ▴ 60
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Comment: C: Control data for chip-seq analysis of SRX681547, SRX681548 data
5.9 years ago by gskbioinfo143 ▴ 60
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Comment: C: Control data for chip-seq analysis of SRX681547, SRX681548 data
5.9 years ago by gskbioinfo143 ▴ 60
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1.3k
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Comment: C: Control data for chip-seq analysis of SRX681547, SRX681548 data
5.9 years ago by gskbioinfo143 ▴ 60
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2.4k
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Comment: C: DiffBind installation error in R & Rstudio?
5.9 years ago by gskbioinfo143 ▴ 60
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5.6k
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Comment: C: Any One please provide protocol for Analysing long noncoding RNA illumina NGS da
6.0 years ago by gskbioinfo143 ▴ 60
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16k
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Comment: C: Software For Hla Typing Using Ngs?
6.5 years ago by gskbioinfo143 ▴ 60
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Comment: C: which is the best software for Sequence based typing(SBT) HLA typing?
6.5 years ago by gskbioinfo143 ▴ 60
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3.4k
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Comment: C: how to design primers for IKBKG gene if it has pseudo gene?
6.6 years ago by gskbioinfo143 ▴ 60
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Comment: C: how to get read group information for bam file of Ion torrent data?
7.0 years ago by gskbioinfo143 ▴ 60
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3.2k
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Comment: C: how to get read group information for bam file of Ion torrent data?
7.0 years ago by gskbioinfo143 ▴ 60
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2.4k
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Comment: C: Where to get chromosome start end positions for this COSMIC IDs?
7.0 years ago by gskbioinfo143 ▴ 60
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2.3k
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Comment: C: How to find out off target reads?
7.1 years ago by gskbioinfo143 ▴ 60
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1.6k
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Comment: C: How to get DEPTH, as well as variant calling of transcriptome data
7.1 years ago by gskbioinfo143 ▴ 60
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Comment: Comment: human transcriptome size
updated 7 months ago by 36k • written 7.1 years ago by ▴ 60
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5.5k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
7.3 years ago by gskbioinfo143 ▴ 60
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1
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5.5k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
7.3 years ago by gskbioinfo143 ▴ 60
0
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1
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5.5k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
7.3 years ago by gskbioinfo143 ▴ 60
0
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1
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5.5k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
7.3 years ago by gskbioinfo143 ▴ 60
0
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1
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5.5k
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Comment: Comment: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
updated 4 weeks ago by 36k • written 7.3 years ago by ▴ 60
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2.8k
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Comment: Comment: Tool to detect Copy Number Variations(CNV) using Single Read End Data
updated 6 weeks ago by 36k • written 7.3 years ago by ▴ 60
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Comment: C: Copy Number Variation (Cnv) Detection Using Single-End Sequencing Data
7.3 years ago by gskbioinfo143 ▴ 60
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865
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Comment: C: Tool to check Number of cells covered in the RNA sample after RNA-Seq analysis?
7.3 years ago by gskbioinfo143 ▴ 60
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Comment: Comment: whre we can get BRCA1 and 2 SNPs data for indian population?
7.4 years ago by gskbioinfo143 ▴ 60
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