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Search results for python rna seq
python
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rna-seq
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112 search results found
Mapp
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7
🗺️ MAPP is a computational method which enables identification of binding motifs for RNA-binding proteins that shape pre-mRNA processing under specific conditions.
Primerseq
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7
Primer Seek in RNA-Seq. Designs RT-PCR primers that validate alternative splicing events from RNA-Seq data.
Sargasso
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6
Sargasso disambiguates mixed-species high-throughput sequencing data.
Pyfeat 2.x
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6
Biological Feature Representation Tool form the Sequences
Curare
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6
Curare - A customizable and reproducible analysis pipeline for RNA-Seq experiments
Socube
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6
A simple python package for doublet detection in scRNA-seq data
Bam Lorenz Coverage
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6
Generate Lorenz plots and Coverage plots directly from BAM files
Caars
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6
CAARS: Comparative Assembly and Annotation of RNA-Seq data
Deepsplice
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6
DeepSplice: Deep Classification of Novel Splice Junctions Revealed by RNA-seq
Rnaseq_workflow
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6
snakemake workflow for bulk RNA-seq workflow using STAR-edgeR
Epydoor
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5
Epitope discovery pipeline for RNA-seq
Metadatatable
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5
Work on and around an interactive metadata table for project identification
Alaska
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5
Automated and friendly RNA-seq analysis (deprecated)
Bento Seq
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5
Bootstrap Estimation Tool for RNA-Seq
Lyric
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5
Long RNA-seq analysis workflow
Utr_add_extend_gtf
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5
Provided tool will add explicit 3'UTR and extends it into a valid Ensembl GTF file. It's useful for 3'RNAseq when 3' coordinates might not be as good as you expect.
Ribo Oddr
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5
Ribo-seq focused Oligo Design pipeline for experiment-specific Depletion of Ribosomal RNAs
Genome_tracks
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5
A Snakemake workflow for easy visualization of genome browser tracks of aligned BAM files powered by the wrapper gtracks for the package pyGenomeTracks.
Clair3 Rna
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5
Clair3-RNA - long-read short variant caller for RNA sequencing data
Splice Q
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5
SPLICE-q -- A Python tool for genome-wide SPLIcing Efficiency quantification from RNA-seq data.
Imrep.gtex
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5
Scripts and commands we used in our study : Profiling immunoglobulin repertoires across multiple human tissues by RNA Sequencing
Rediscover
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5
RNA editing discovery from NGS data.
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