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Comment: C: how to design primers for IKBKG gene if it has pseudo gene?
updated 4.4 years ago by 43k • written 8.3 years ago by ▴ 60
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Comment: C: how to design primers for IKBKG gene if it has pseudo gene?
updated 4.4 years ago by 43k • written 8.3 years ago by ▴ 60
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Comment: C: Where to get chromosome start end positions for this COSMIC IDs?
updated 4.5 years ago by 43k • written 8.7 years ago by ▴ 60
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Comment: C: Where to get chromosome start end positions for this COSMIC IDs?
updated 4.5 years ago by 43k • written 8.7 years ago by ▴ 60
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Comment: C: How to convert fastq file with raw reads to draft genome fastq file ?
7.0 years ago by gskbioinfo143 ▴ 60
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Comment: C: How to convert fastq file with raw reads to draft genome fastq file ?
7.0 years ago by gskbioinfo143 ▴ 60
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Comment: C: How to do Genome Annotation?
7.1 years ago by gskbioinfo143 ▴ 60
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Comment: C: peakannotation by peakAnalyzer
7.3 years ago by gskbioinfo143 ▴ 60
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Comment: C: Quality check of Medip Seq Data
7.4 years ago by gskbioinfo143 ▴ 60
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2.3k
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Comment: C: Quality check of Medip Seq Data
7.4 years ago by gskbioinfo143 ▴ 60
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2.3k
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Comment: C: Quality check of Medip Seq Data
7.4 years ago by gskbioinfo143 ▴ 60
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Comment: C: Control data for chip-seq analysis of SRX681547, SRX681548 data
7.6 years ago by gskbioinfo143 ▴ 60
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Comment: C: Control data for chip-seq analysis of SRX681547, SRX681548 data
7.6 years ago by gskbioinfo143 ▴ 60
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1.8k
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Comment: C: Control data for chip-seq analysis of SRX681547, SRX681548 data
7.6 years ago by gskbioinfo143 ▴ 60
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3.1k
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Comment: C: DiffBind installation error in R & Rstudio?
7.6 years ago by gskbioinfo143 ▴ 60
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6.4k
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Comment: C: Any One please provide protocol for Analysing long noncoding RNA illumina NGS da
7.7 years ago by gskbioinfo143 ▴ 60
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Comment: C: Software For Hla Typing Using Ngs?
8.2 years ago by gskbioinfo143 ▴ 60
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Comment: C: which is the best software for Sequence based typing(SBT) HLA typing?
8.2 years ago by gskbioinfo143 ▴ 60
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4.2k
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Comment: C: how to design primers for IKBKG gene if it has pseudo gene?
8.3 years ago by gskbioinfo143 ▴ 60
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6.1k
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Comment: Comment: How to get read group information for bam file
updated 18 months ago by 43k • written 8.7 years ago by ▴ 60
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6.1k
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Comment: Comment: How to get read group information for bam file
updated 18 months ago by 43k • written 8.7 years ago by ▴ 60
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3.0k
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Comment: Comment: Where to get chromosome start end positions for this COSMIC IDs?
updated 18 months ago by 43k • written 8.7 years ago by ▴ 60
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2.6k
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Comment: C: How to find out off target reads?
8.8 years ago by gskbioinfo143 ▴ 60
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2.0k
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Comment: C: How to get DEPTH, as well as variant calling of transcriptome data
8.8 years ago by gskbioinfo143 ▴ 60
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6.0k
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Comment: Comment: human transcriptome size
updated 2.3 years ago by 43k • written 8.8 years ago by ▴ 60
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6.1k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
9.0 years ago by gskbioinfo143 ▴ 60
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1
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6.1k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
9.0 years ago by gskbioinfo143 ▴ 60
0
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1
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6.1k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
9.0 years ago by gskbioinfo143 ▴ 60
0
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1
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6.1k
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Comment: C: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
9.0 years ago by gskbioinfo143 ▴ 60
0
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1
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6.1k
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Comment: Comment: Bedtools Genomecoveragebed Usage : How To do per base coverage analysis for only
updated 21 months ago by 43k • written 9.0 years ago by ▴ 60
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3.0k
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Comment: Comment: Tool to detect Copy Number Variations(CNV) using Single Read End Data
updated 22 months ago by 43k • written 9.0 years ago by ▴ 60
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Comment: C: Copy Number Variation (Cnv) Detection Using Single-End Sequencing Data
9.0 years ago by gskbioinfo143 ▴ 60
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1.1k
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Comment: C: Tool to check Number of cells covered in the RNA sample after RNA-Seq analysis?
9.1 years ago by gskbioinfo143 ▴ 60
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2.4k
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Comment: Comment: whre we can get BRCA1 and 2 SNPs data for indian population?
9.1 years ago by gskbioinfo143 ▴ 60
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