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Comment: Comment: How to create a basic GUI for rna seq pipeline
2.2 years ago by sbt_gvs • 0
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Comment: Comment: Aberrant splicing in bulk RNAseq
2.3 years ago by sbt_gvs • 0
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Comment: Comment: Merging FASTQ files with Cellranger
2.5 years ago by sbt_gvs • 0
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Comment: Comment: Meaning of TCGA CNV data
2.9 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
2.9 years ago by sbt_gvs • 0
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Comment: Comment: how to interpret a CNV scatter plot
2.9 years ago by sbt_gvs • 0
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Comment: Comment: Analyzing proteomics data
3.3 years ago by sbt_gvs • 0
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Proteomics to pathway data analysis R and Python packages
pathway proteomics normalized
3.3 years ago by sbt_gvs • 0
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