About Anaconda Help Download Anaconda

genomedk / packages

Package Name Access Summary Updated
ucsc-nettoaxt-ramstein public Convert net (and chain) to axt. 2023-06-16
bayescan public Phylogenetics - Randomized Axelerated Maximum Likelihood. 2023-06-16
r-diversitree public Contains a number of comparative 'phylogenetic' methods, mostly focusing on analysing diversification and character evolution. Contains implementations of 'BiSSE' (Binary State 'Speciation' and Extinction) and its unresolved tree extensions, 'MuSSE' (Multiple State 'Speciation' and Extinction), 'QuaSSE', 'GeoSSE', and 'BiSSE-ness' Other included methods include Markov models of discrete and continuous trait evolution and constant rate 'speciation' and extinction. 2023-06-16
psmc public Pairwise Sequentially Markovian Coalescent 2023-06-16
snoreport public SnoReport 2.0: new features and a refined Support Vector Machine to improve snoRNA identification 2023-06-16
stacks public Stacks is a software pipeline for building loci from RAD-seq 2023-06-16
r-lava-jw public Melds genome-wide association tests with structural equation modeling (SEM) using 'OpenMx'. This package contains low-level C/C++ code to rapidly read genetic data encoded in U.K. Biobank or 'plink' formats. Prebuilt modeling options include one and two factor models. Alternately, analyses may utilize arbitrary, user-provided SEMs. See Verhulst, Maes, & Neale (2017) <doi:10.1007/s10519-017-9842-6> for details. An updated manuscript is in preparation. 2023-06-16
r-matrixsampling public Provides samplers for various matrix variate distributions: Wishart, inverse-Wishart, normal, t, inverted-t, Beta type I, Beta type II, Gamma, confluent hypergeometric. Allows to simulate the noncentral Wishart distribution without the integer restriction on the degrees of freedom. 2023-06-16
r-superfreq public SuperFreq analyses SNVs and CNAs of multiple cancer exomes, sharing all information across samples and mutation types. The inputs are the bam-files and a preliminary SNV calling in .vcf format. SuperFreq filters and annotates the SNVs, calls CNAs and tracks clones over samples from the same individual. A matched normal improves results, but is not necessary. SuperFreq requireas at least two (preferably 5-10 or more) reference normal samples that do not have to be related to the studied cancer samples, but must be from the same sequencing platform and capture. These are used to improve results through variance of read depth and requrring false SNVs amongst other things. SuperFreq produces ample output in terms of plots and spread sheets, both for identifying properties of the cancer samples and for quality control. 2023-06-16
r-gwsem public Melds genome-wide association tests with structural equation modeling (SEM) using 'OpenMx'. This package contains low-level C/C++ code to rapidly read genetic data encoded in U.K. Biobank or 'plink' formats. Prebuilt modeling options include one and two factor models. Alternately, analyses may utilize arbitrary, user-provided SEMs. See Verhulst, Maes, & Neale (2017) <doi:10.1007/s10519-017-9842-6> for details. An updated manuscript is in preparation. 2023-06-16
seq-lang public A strongly-typed and statically-compiled high-performance Pythonic language! 2023-06-16
r-diem public Identification of debris-containing droplets from a droplet-based single cell/nucleus RNA-seq. 'diem' classifies droplets by modeling droplet expression with a multinomial mixture model. Droplets are assigned to debris or cell type clusters after estimating parameters with expectation maximization (EM). Provides quantifications of contamination in individual droplets for filtering and use as a covariate. See Alvarez M, Rahmani E, et al (2019) <doi:10.1101/786285> for details. 2023-06-16
treepl public Phylogenetic penalized likelihood 2023-06-16
rnahybrid public RNAhybrid is a tool for finding the minimum free energy hybridization of a long and a short RNA. 2023-06-16
primer3 public Design PCR primers from DNA sequence. From mispriming libraries to sequence quality data to the generation of internal oligos, primer3 does it. 2023-06-16
exabayes public ExaBayes is a software package for Bayesian tree inference. It is particularly suitable for large-scale analyses on computer clusters. 2023-06-16
fdstools public Forensic DNA Sequencing Tools 2023-06-16
phyx public No Summary 2023-06-16
epacts public No Summary 2023-06-16
regenie public whole genome regression modelling of large genome-wide association studies 2023-06-16
singularity public Singularity: Application containers for Linux 2023-06-16
grapes-static public Rate of Adaptive Protein Evolution Software 2023-06-16
argweaver public Sampling and manipulating genome-wide ancestral recombination graphs (ARGs) 2023-06-16
maffilter public The MafFilter genome alignment processor 2023-06-16
phusion2-crossgenome public No Summary 2023-06-16
redundans public No Summary 2023-06-16
r-ggimage public Supports image files and graphic objects to be visualized in 'ggplot2' graphic system. 2023-06-16
r-qgraph public Weighted network visualization and analysis, as well as Gaussian graphical model computation. See Epskamp et al. (2012) <doi:10.18637/jss.v048.i04>. 2023-06-16
rvtests public Rare variant test software for next generation sequencing data 2023-06-16
r-groupdata2 public Methods for dividing data into groups. Create balanced partitions and cross-validation folds. Perform time series windowing and general grouping and splitting of data. Balance existing groups with up- and downsampling. 2023-06-16
hyphy public An open-source software package for comparative sequence analysis using stochastic evolutionary models. 2023-06-16
abra2 public ABRA2 is an updated implementation of ABRA featuring 2023-06-16
raremetal public No Summary 2023-06-16
r-hdpca public In high-dimensional settings: Estimate the number of distant spikes based on the Generalized Spiked Population (GSP) model. Estimate the population eigenvalues, angles between the sample and population eigenvectors, correlations between the sample and population PC scores, and the asymptotic shrinkage factors. Adjust the shrinkage bias in the predicted PC scores. 2023-06-16
ldak5-parallel public No Summary 2023-06-16
r-bigutilsr public Utility functions for large-scale data. For now, package 'bigutilsr' mainly includes functions for outlier detection. 2023-06-16
ldak5 public No Summary 2023-06-16
cget public Cmake package retrieval 2023-06-16
perl-digest-sha1 public Perl interface to the SHA-1 algorithm 2023-06-16
perl public No Summary 2023-06-16
perl-file-map public Memory mapping made simple and safe. 2023-06-16
perl-extutils-cbuilder public Compile and link C code for Perl modules 2023-06-16
perl-convert-uu public perl replacement for uudecode 2023-06-16
perl-perlio-layers public Querying your filehandle's capabilities 2023-06-16
perl-mock-config public temporarily set Config or XSConfig values 2023-06-16
perl-devel-checklib public check that a library is available 2023-06-16
perl-io-captureoutput public capture STDOUT and STDERR from Perl code, subprocesses or XS 2023-06-16
r public No Summary 2023-06-16
gdk-ssl-cert public No Summary 2023-06-16
finestructure public No Summary 2023-06-16

© 2024 Anaconda, Inc. All Rights Reserved. (v4.0.6) Legal | Privacy Policy