Manoj Kumar Valluru (vallurumk)

vallurumk

Geek Repo

Company:University of Sheffield

Location:Sheffield, UK

Twitter:@mkvalluru

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Manoj Kumar Valluru's repositories

awesome-pipeline

A curated list of awesome pipeline toolkits inspired by Awesome Sysadmin

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bcbio-nextgen

Validated, scalable, community developed variant calling, RNA-seq and small RNA analysis

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bhtsne

Barnes-Hut t-SNE

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biojupies

Automated generation of tailored bioinformatics Jupyter Notebooks via a user interface.

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cloudbiolinux

CloudBioLinux: configure virtual (or real) machines with tools for biological analyses

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common-workflow-language

Repository for the CWL standards. Use https://www.biostars.org/t/cwl/ for support 😊

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cwl-website

www.commonwl.org

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DeepPATH

Classification of Lung cancer slide images using deep-learning

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deepvariant

Google's DeepVariant variant caller as a Nextflow pipeline

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EnhancedVolcano

Publication-ready volcano plots with enhanced colouring and labeling

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guessing_game

UNIX WORKBENCH Peer-graded Assignment

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hpcuk-website

Source for the HPC-UK website

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iCLIPlib

Tools for dealing with iCLIP data

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igv

Integrative Genomics Viewer. Fast, efficient, scalable visualization tool for genomics data and annotations

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IsoformSwitchAnalyzeR

An R package to Identify, Annoatate and Visialize Isoform Switches with Functional Consequences (from RNA-seq data)

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keras-gcnn

Roto-reflection equivariant CNNs for Keras as presented in B. S. Veeling, J. Linmans, J. Winkens, T. Cohen, M. Welling. "Rotation Equivariant CNNs for Digital Pathology".

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lncpipe

UNDER DEVELOPMENT--- A Nextflow-based pipeline for comprehensive analyses of long non-coding RNAs from RNA-seq datasets

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Multicore-TSNE

Parallel t-SNE implementation with Python and Torch wrappers.

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pandas

Flexible and powerful data analysis / manipulation library for Python, providing labeled data structures similar to R data.frame objects, statistical functions, and much more

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parliament2

Runs a combination of tools to generate structural variant calls on whole-genome sequencing data

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pathology-images-analysis-using-CNN

Scripts for https://www.nature.com/articles/s41598-018-27707-4, using Convolutional Neural Network to detect lung cancer tumor area

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RainCloudPlots

Code and tutorials to visualise your data that is both beautiful *and* statistically valid

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raw

The missing link between spreadsheets and data visualization

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ReproduciblePython

Workshop materials for PyCon 2018 workshop on reproducible analysis in Python

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rna-seq-pipeline

WDL_RNA-Seq_star_rsem

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rnafusion

RNA-seq analysis pipeline for detection gene-fusions

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the-unix-workbench

:house_with_garden: A Book for Anyone to Get Started with Unix

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toil

A scalable, efficient, cross-platform and easy-to-use workflow engine in pure Python

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TPMCalculator

TPMCalculator quantifies mRNA abundance directly from the alignments by parsing BAM files

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