sophy7074 Goto Github PK

acnviewer

Comprehensive genome-wide visualization of absolute copy number and copy neutral variations

autocnv

some changes for use

autopvs1

An automatic classification tool for PVS1 interpretation of null variants

awesome-deeplearning

深度学习入门课、资深课、特色课、学术案例、产业实践案例、深度学习知识百科及面试题库The course, case and knowledge of Deep Learning and AI

awesome-genome-visualization

A list of interesting genome browser or genome-browser-like implementations

bio-pipeline

My collection of light bioinformatics analysis pipelines for specific tasks

biocommons.seqrepo

non-redundant, compressed, journalled, file-based storage for biological sequences

bioinformatics-training

Bioinformatics training resources

carrot

这儿为你准备了众多免费好用的ChatGPT镜像站点，当前100+站点

cnara

Reliability assessment for genomic copy number profiles

cnvkit

Copy number variant detection from targeted DNA sequencing - test by sophy7074

cnvpytor

a python extension of CNVnator -- a tool for CNV analysis from depth-of-coverage by mapped reads

cwltool

Common Workflow Language reference implementation

daligner

Find all significant local alignments between reads

dash

Data Apps & Dashboards for Python. No JavaScript Required.

datasciencecoursera

This is for Data Scientist

datasharing

The Leek group guide to data sharing

dazz_db

The Dazzler Data Base

decon

downloaddata

easy-scraping-tutorial

Simple but useful Python web scraping tutorial code.

ebooks

eBook分享大集合：主要以IT领域经典书籍收藏，以备不时之需。

echarts

Enterprise Charts | Github pages : http://ecomfe.github.io/echarts/index-en.html | Email : [email protected] | Baidu Hi : 1379172 |

ectools

tools for error correction and working with long read data

example

exomiser

A Tool to Annotate and Prioritize Exome Variants - test by sophy7074

falcon

FALCON: experimental PacBio diploid assembler

filtus

genbank2gtf

genomicconsensus

PacBio® variant and consensus caller (Quiver algorithm)