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artieri_et_al_nips_at_low_ff icon artieri_et_al_nips_at_low_ff

Code required to reproduce the results of Artieri et al. "Noninvasive Prenatal Screening at Low Fetal Fraction: Comparing Whole-Genome Sequencing and Single-Nucleotide Polymorphism Methods"

bcbio-nextgen icon bcbio-nextgen

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

bioinfotools icon bioinfotools

Documenting usage and experience with bioinformatic tools

cava icon cava

CAVA (Clinical Annotation of VAriants)

cfdna icon cfdna

Analysis of epigenetic signals captured by fragmentation patterns of cell-free DNA

cfdnapipe icon cfdnapipe

A comprehensive cell free DNA quality control and analysis pipeline

clinicalgradednaseq icon clinicalgradednaseq

Automated next generation DNA sequencing analysis pipeline suited for clinical tests, with >99.9% sensitivity to Sanger sequencing at read-depth>18

cnvkit icon cnvkit

Copy number variant detection from targeted DNA sequencing

crack-js icon crack-js

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deepnudes icon deepnudes

Cracked version of DeepNudes software with everything working, free for download (Magnet Link)

deepvariant icon deepvariant

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

diabetes-prediction-2.0 icon diabetes-prediction-2.0

Diabetes prediction V2.0 -This VB6 application takes glycemic values and tries to predict the future state of the patient. First, it converts a sequence of numbers into states. The states are arranged in a transition matrix and the transition probabilities are calculated for each element. The transition matrix is further used for a predictions.

expert_readed_books icon expert_readed_books

2021年最新总结,推荐工程师合适读本,计算机科学,软件技术,创业,**类,数学类,人物传记书籍

fetalfraction icon fetalfraction

Computational Estimation of Fetal DNA Fraction in Low Coverage Whole Genome Sequencing Data

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