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Comment: C: how to design primers for IKBKG gene if it has pseudo gene?
updated 3.8 years ago by 40k • written 7.8 years ago by ▴ 60
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Comment: C: how to design primers for IKBKG gene if it has pseudo gene?
updated 3.8 years ago by 40k • written 7.8 years ago by ▴ 60
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Comment: C: Where to get chromosome start end positions for this COSMIC IDs?
updated 3.9 years ago by 40k • written 8.2 years ago by ▴ 60
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Comment: C: Where to get chromosome start end positions for this COSMIC IDs?
updated 3.9 years ago by 40k • written 8.2 years ago by ▴ 60
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Comment: C: How to convert fastq file with raw reads to draft genome fastq file ?
6.4 years ago by gskbioinfo143 ▴ 60
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Comment: C: How to convert fastq file with raw reads to draft genome fastq file ?
6.4 years ago by gskbioinfo143 ▴ 60
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Comment: C: How to do Genome Annotation?
6.5 years ago by gskbioinfo143 ▴ 60
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Comment: C: peakannotation by peakAnalyzer
6.7 years ago by gskbioinfo143 ▴ 60
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Comment: C: Quality check of Medip Seq Data
6.8 years ago by gskbioinfo143 ▴ 60
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2.1k
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Comment: C: Quality check of Medip Seq Data
6.8 years ago by gskbioinfo143 ▴ 60
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2.1k
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Comment: C: Quality check of Medip Seq Data
6.8 years ago by gskbioinfo143 ▴ 60
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Comment: C: Control data for chip-seq analysis of SRX681547, SRX681548 data
7.0 years ago by gskbioinfo143 ▴ 60
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Comment: C: Control data for chip-seq analysis of SRX681547, SRX681548 data
7.0 years ago by gskbioinfo143 ▴ 60
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1.6k
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Comment: C: Control data for chip-seq analysis of SRX681547, SRX681548 data
7.1 years ago by gskbioinfo143 ▴ 60
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2.9k
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Comment: C: DiffBind installation error in R & Rstudio?
7.1 years ago by gskbioinfo143 ▴ 60
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Comment: C: Any One please provide protocol for Analysing long noncoding RNA illumina NGS da
7.1 years ago by gskbioinfo143 ▴ 60
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Comment: C: Software For Hla Typing Using Ngs?
7.7 years ago by gskbioinfo143 ▴ 60
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Comment: C: which is the best software for Sequence based typing(SBT) HLA typing?
7.7 years ago by gskbioinfo143 ▴ 60
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3.9k
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Comment: C: how to design primers for IKBKG gene if it has pseudo gene?
7.8 years ago by gskbioinfo143 ▴ 60
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5.1k
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Comment: Comment: How to get read group information for bam file
updated 11 months ago by 40k • written 8.2 years ago by ▴ 60
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5.1k
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Comment: Comment: How to get read group information for bam file
updated 11 months ago by 40k • written 8.2 years ago by ▴ 60
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2.8k
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Comment: Comment: Where to get chromosome start end positions for this COSMIC IDs?
updated 11 months ago by 40k • written 8.2 years ago by ▴ 60
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2.5k
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Comment: C: How to find out off target reads?
8.2 years ago by gskbioinfo143 ▴ 60
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1.8k
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Comment: C: How to get DEPTH, as well as variant calling of transcriptome data
8.3 years ago by gskbioinfo143 ▴ 60
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Comment: Comment: human transcriptome size
updated 21 months ago by 40k • written 8.3 years ago by ▴ 60
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5.9k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
8.5 years ago by gskbioinfo143 ▴ 60
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1
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5.9k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
8.5 years ago by gskbioinfo143 ▴ 60
0
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1
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5.9k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
8.5 years ago by gskbioinfo143 ▴ 60
0
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1
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5.9k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
8.5 years ago by gskbioinfo143 ▴ 60
0
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1
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5.9k
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Comment: Comment: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
updated 15 months ago by 40k • written 8.5 years ago by ▴ 60
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2.9k
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Comment: Comment: Tool to detect Copy Number Variations(CNV) using Single Read End Data
updated 15 months ago by 40k • written 8.5 years ago by ▴ 60
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Comment: C: Copy Number Variation (Cnv) Detection Using Single-End Sequencing Data
8.5 years ago by gskbioinfo143 ▴ 60
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Comment: C: Tool to check Number of cells covered in the RNA sample after RNA-Seq analysis?
8.5 years ago by gskbioinfo143 ▴ 60
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Comment: Comment: whre we can get BRCA1 and 2 SNPs data for indian population?
8.5 years ago by gskbioinfo143 ▴ 60
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