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Comment: Comment: How to create a basic GUI for rna seq pipeline
17 months ago by sbt_gvs • 0
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Comment: Comment: Aberrant splicing in bulk RNAseq
20 months ago by sbt_gvs • 0
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Comment: Comment: Merging FASTQ files with Cellranger
22 months ago by sbt_gvs • 0
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Comment: Comment: Meaning of TCGA CNV data
2.2 years ago by sbt_gvs • 0
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Comment: Comment: What is probe number and segmentation mean in copy number variation(CNV) data
2.2 years ago by sbt_gvs • 0
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Comment: Comment: how to interpret a CNV scatter plot
2.2 years ago by sbt_gvs • 0
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Comment: Comment: Analyzing proteomics data
2.6 years ago by sbt_gvs • 0
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Proteomics to pathway data analysis R and Python packages
pathway proteomics normalized
2.6 years ago by sbt_gvs • 0
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