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bioconda / packages

Package Name Access Summary Updated
teloclip public A tool for the recovery of unassembled telomeres from soft-clipped read alignments. 2025-04-22
perl-sys-info public Fetch information from the host system 2025-04-22
perl-sys-info-driver-osx public OSX driver for Sys::Info 2025-04-22
perl-mac-propertylist public work with Mac plists at a low level 2025-04-22
perl-xml-entities public Mapping of XML entities to Unicode 2025-04-22
perl-math-random-mt-auto public Auto-seeded Mersenne Twister PRNGs 2025-04-22
perl-parallel-loops public Execute loops using parallel forked subprocesses 2025-04-22
perl-object-insideout public Comprehensive inside-out object support module 2025-04-22
perl-math-bigint public Arbitrary size floating point math package 2025-04-22
perl-math-complex public trigonometric functions 2025-04-22
crux-toolkit public A cross-platform suite of analysis tools for interpreting protein mass spectrometry data 2025-04-22
focus public FOCUS is an innovative and agile model to profile and report organisms present in metagenomic samples based on composition usage without sequence length dependencies. 2025-04-22
perl-sys-info-driver-linux public Linux driver for Sys::Info 2025-04-22
perl-devel-assert public assertions for Perl >= 5.14 2025-04-22
perl-test-sys-info public Centralized test suite for Sys::Info. 2025-04-22
perl-sys-info-base public Base class for Sys::Info 2025-04-22
strike public A program to evaluate protein multiple sequence alignments using a single protein structure. 2025-04-22
collect_mgf public Collects MGF files and dd_results from an XMass setup_QDD.tcl experiment to a single MGF file. 2025-04-22
clairvoyante public Identifying the variants of DNA sequences sensitively and accurately is an important but challenging task in the field of genomics. This task is particularly difficult when dealing with Single Molecule Sequencing, the error rate of which is still tens to hundreds of times higher than Next Generation Sequencing. With the increasing prevalence of Single Molecule Sequencing, an efficient variant caller will not only expedite basic research but also enable various downstream applications. To meet this demand, we developed Clairvoyante, a multi-task five-layer convolutional neural network model for predicting variant type, zygosity, alternative allele and Indel length. On NA12878, Clairvoyante achieved 99.73%, 97.68% and 95.36% accuracy on known variants, and achieved 98.65%, 92.57%, 77.89% F1 score on the whole genome, in Illumina, PacBio, and Oxford Nanopore data, respectively. Training Clairvoyante with a sample and call variant on another shows that Clairvoyante is sample agnostic and general for variant calling. A slim version of Clairvoyante with reduced model parameters produced a much lower F1, suggesting the full model's power in disentangling subtle details in read alignment. Clairvoyante is the first method for Single Molecule Sequencing to finish a whole genome variant calling in two hours on a 28 CPU-core machine, with top-tier accuracy and sensitivity. A toolset was developed to train, utilize and visualize the Clairvoyante model easily, and is publically available here is this repo. 2025-04-22
mapdia public Performs essential data preprocessing, including novel retention time-based normalization method and a sequence of peptide/fragment selection steps, and more importantly, hierarchical model-based statistical significance analysis for multi-group comparisons under representative experimental designs. 2025-04-22
perl-business-isbn public work with International Standard Book Numbers 2025-04-22
perl-business-isbn-data public data pack for Business::ISBN 2025-04-22
somaticseq public An ensemble approach to accurately detect somatic mutations. 2025-04-22
starfish public Standardized analysis pipeline for image-based transcriptomics. 2025-04-22
slicedimage public Python module to access sliced imaging data 2025-04-22

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