Pengyao Ping (Jappy0)

Jappy0

Geek Repo

Company:University of Technology Sydney

Location:Sydney

Home Page:https://jappy0.github.io/Jappy/

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Pengyao Ping's repositories

NBCLDA

A Novel Probability Model for LncRNA–Disease Association Prediction Based on the Naïve Bayesian Classifier

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microbe-drug-disease

Predicting pairwise relationships between human microbes, drugs and diseases

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AAva-20-21-P2

Second Project of our Advanced Algorithms course, on the Common Substrings of More Than Two Strings problem

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bioconda-recipes

Conda recipes for the bioconda channel.

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biotite

A comprehensive library for computational molecular biology

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ccs

CCS: Generate Highly Accurate Single-Molecule Consensus Reads (HiFi Reads)

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CoLoRd

A versatile compressor of third generation sequencing reads.

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Deduplication_ErrorCorrection

How error correction affects PCR deduplication: a survey based on UMI datasets of short reads

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deepconsensus

DeepConsensus uses gap-aware sequence transformers to correct errors in Pacific Biosciences (PacBio) Circular Consensus Sequencing (CCS) data.

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DPKL

Code accompanying the UAI 2021 paper 'Deep Kernels with Probabilistic Embeddings for Small-Data Learning'

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hifiasm

Hifiasm: a haplotype-resolved assembler for accurate Hifi reads

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Jappy

Jappy Ping

MathFeature

Feature Extraction Package for Biological Sequences

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miREC

An error correction tool for miRNA reads at single-base resolution

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pbbam

PacBio BAM C++ library

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reads2graph

Edit-distance-based read graph construction from short reads

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readSimulator

Simulating paired-end short sequencing reads from circular and linear genomes

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seqgendiff

Sequence Generation for Differential Expression Analysis and Beyond

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setuptools

Official project repository for the Setuptools build system

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strain_identify

repo for strain identification project

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VariantWorks

Deep Learning based variant calling toolkit - https://clara-parabricks.github.io/VariantWorks/

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XICRA

Small RNAseq pipeline for paired-end reads

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Jappy0

Personal repository

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noise2reads

Accurate and fast error correction and deduplication on short-read sequencing data

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