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c_amps-prediction

crispr_toolkit

CRISPR Indel, base edit analysis

crisprdisco

CRISPR discovery pipeline

crispresso

Software pipeline for the analysis of CRISPR-Cas9 genome editing outcomes from sequencing data

crispresso2

Analysis of deep sequencing data for rapid and intuitive interpretation of genome editing experiments

crispridentify

crisprloci

crisproff

off-targeting assessment of Cas9 gRNAs

crispron

CRISPR Cas9 ontarget prediction software

crisprvariants

crisprviz

A CRISPR repeat|spacer analysis tool

crop-seq

Data analysis scripts for Datlinger et. al, 2017 (doi:10.1038/nmeth.4177)

dalle-mini

DALL·E Mini - Generate images from a text prompt

data-expts

dbparser

Source code for the R package, "dbparser" (i.e. DrugBank Parser)

deal_drugbank

Python xml.sax

deblur

Deblur is a greedy deconvolution algorithm based on known read error profiles.

dedup

A merged read deduplication tool capable to perform merged read deduplication on single end data.

deep-learning-with-pytorch

Deep Learning with PyTorch, published by Packt

deepcrispr

deepest-fusion

DEEPEST-Fusion is a fusion detection algorithm specially designed for screening massive cancer sequencing databases

deephf

Core code for the DeepHF prediction tool

deeplearning-500-questions

深度学习500问，以问答形式对常用的概率知识、线性代数、机器学习、深度学习、计算机视觉等热点问题进行阐述，以帮助自己及有需要的读者。 全书分为18个章节，50余万字。由于水平有限，书中不妥之处恳请广大读者批评指正。 未完待续............ 如有意合作，联系[email protected] 版权所有，违权必究 Tan 2018.06

deeprank

deepvariant

DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.

detect-seq

An unbiased method for genome-wide CBE off-targets assessment

dgidb

Rails frontend to The Genome Institute's drug gene interaction database.

digenome-toolkit

Digenome Toolkit

digenome-toolkit2

Digenome-toolkit ver2.

digenomitas

Digenome software