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Package Name Access Summary Updated
bioconductor-ideoviz public Plots data (continuous/discrete) along chromosomal ideogram 2023-12-22
bioconductor-chipenrich.data public Companion package to chipenrich 2023-12-22
bioconductor-trnascanimport public Importing a tRNAscan-SE result file as GRanges object 2023-12-22
bioconductor-hitc public High Throughput Chromosome Conformation Capture analysis 2023-12-22
bioconductor-chipanalyser public ChIPanalyser: Predicting Transcription Factor Binding Sites 2023-12-22
bioconductor-hiannotator public Functions for annotating GRanges objects 2023-12-22
bioconductor-mmdiff2 public Statistical Testing for ChIP-Seq data sets 2023-12-22
bioconductor-gothic public Binomial test for Hi-C data analysis 2023-12-22
bioconductor-starbiotrek public StarBioTrek 2023-12-22
bioconductor-cexor public An R package to uncover high-resolution protein-DNA interactions in ChIP-exo replicates 2023-12-22
bioconductor-mira public Methylation-Based Inference of Regulatory Activity 2023-12-22
bioconductor-sparsesignatures public SparseSignatures 2023-12-22
bioconductor-cemitool public Co-expression Modules identification Tool 2023-12-22
bioconductor-fccac public functional Canonical Correlation Analysis to evaluate Covariance between nucleic acid sequencing datasets 2023-12-22
bioconductor-methylseekr public Segmentation of Bis-seq data 2023-12-22
bioconductor-sevenc public Computational Chromosome Conformation Capture by Correlation of ChIP-seq at CTCF motifs 2023-12-22
bioconductor-excluster public ExCluster robustly detects differentially expressed exons between two conditions of RNA-seq data, requiring at least two independent biological replicates per condition 2023-12-22
bioconductor-methylinheritance public Permutation-Based Analysis associating Conserved Differentially Methylated Elements Across Multiple Generations to a Treatment Effect 2023-12-22
bioconductor-seqsetvis public Set Based Visualizations for Next-Gen Sequencing Data 2023-12-22
bioconductor-bsseqdata public Example whole genome bisulfite data for the bsseq package 2023-12-22
bioconductor-segmentseq public Methods for identifying small RNA loci from high-throughput sequencing data 2023-12-22
bioconductor-methinheritsim public Simulating Whole-Genome Inherited Bisulphite Sequencing Data 2023-12-22
bioconductor-snplocs.hsapiens.dbsnp150.grch38 public SNP locations and alleles for Homo sapiens extracted from NCBI dbSNP Build 150. The source data files used for this package were created by NCBI between March 12-14, 2017, and contain SNPs mapped to reference genome GRCh38.p7 (a patched version of GRCh38 that doesn't alter chromosomes 1-22, X, Y, MT). Note that these SNPs can be "injected" in BSgenome.Hsapiens.NCBI.GRCh38 or in BSgenome.Hsapiens.UCSC.hg38. 2023-12-22
bioconductor-eatonetalchipseq public ChIP-seq data of ORC-binding sites in Yeast excerpted from Eaton et al. 2010 2023-12-22
bioconductor-biseq public Processing and analyzing bisulfite sequencing data 2023-12-22
bioconductor-dmchmm public Differentially Methylated CpG using Hidden Markov Model 2023-12-22
bioconductor-snplocs.hsapiens.dbsnp149.grch38 public SNP locations and alleles for Homo sapiens extracted from NCBI dbSNP Build 149. The source data files used for this package were created by NCBI between November 8-12, 2016, and contain SNPs mapped to reference genome GRCh38.p7 (a patched version of GRCh38 that doesn't alter chromosomes 1-22, X, Y, MT). Note that these SNPs can be "injected" in BSgenome.Hsapiens.NCBI.GRCh38 or in BSgenome.Hsapiens.UCSC.hg38. 2023-12-22
bioconductor-beat public BEAT - BS-Seq Epimutation Analysis Toolkit 2023-12-22
bioconductor-desousa2013 public Poor prognosis colon cancer is defined by a molecularly distinct subtype and precursor lesion 2023-12-22
bioconductor-basecallqc public Working with Illumina Basecalling and Demultiplexing input and output files 2023-12-22
bioconductor-snplocs.hsapiens.dbsnp144.grch38 public SNP locations and alleles for Homo sapiens extracted from NCBI dbSNP Build 144. The source data files used for this package were created by NCBI on May 30, 2015, and contain SNPs mapped to reference genome GRCh38.p2 (a patched version of GRCh38 that doesn't alter chromosomes 1-22, X, Y, MT). Note that these SNPs can be "injected" in BSgenome.Hsapiens.NCBI.GRCh38 or in BSgenome.Hsapiens.UCSC.hg38. 2023-12-22
bioconductor-ballgown public Flexible, isoform-level differential expression analysis 2023-12-22
bioconductor-leebamviews public leeBamViews -- multiple yeast RNAseq samples excerpted from Lee 2009 2023-12-22
bioconductor-snplocs.hsapiens.dbsnp144.grch37 public SNP locations and alleles for Homo sapiens extracted from NCBI dbSNP Build 144. The source data files used for this package were created by NCBI on May 29-30, 2015, and contain SNPs mapped to reference genome GRCh37.p13. WARNING: Note that the GRCh37.p13 genome is a patched version of GRCh37. However the patch doesn't alter chromosomes 1-22, X, Y, MT. GRCh37 itself is the same as the hg19 genome from UCSC *except* for the mitochondrion chromosome. Therefore, the SNPs in this package can be "injected" in BSgenome.Hsapiens.UCSC.hg19 and they will land at the correct position but this injection will exclude chrM (i.e. nothing will be injected in that sequence). 2023-12-22
bioconductor-coverageview public Coverage visualization package for R 2023-12-22
bioconductor-rtrmui public A shiny user interface for rTRM 2023-12-22
bioconductor-xtrasnplocs.hsapiens.dbsnp144.grch38 public Extra SNP locations and alleles for Homo sapiens extracted from NCBI dbSNP Build 144. The source data files used for this package were created by NCBI on May 30, 2015, and contain SNPs mapped to reference genome GRCh38.p2 (a patched version of GRCh38 that doesn't alter chromosomes 1-22, X, Y, MT). While the SNPlocs.Hsapiens.dbSNP144.GRCh38 package contains only molecular variations of class "snp", this package contains molecular variations of other classes (in-del, heterozygous, microsatellite, named-locus, no-variation, mixed, and multinucleotide-polymorphism). 2023-12-22
bioconductor-xtrasnplocs.hsapiens.dbsnp144.grch37 public Extra SNP locations and alleles for Homo sapiens extracted from NCBI dbSNP Build 144. The source data files used for this package were created by NCBI on May 29-30, 2015, and contain SNPs mapped to reference genome GRCh37.p13 (a patched version of GRCh37 that doesn't alter chromosomes 1-22, X, Y, MT). While the SNPlocs.Hsapiens.dbSNP144.GRCh37 package contains only molecular variations of class "snp", this package contains molecular variations of other classes (in-del, heterozygous, microsatellite, named-locus, no-variation, mixed, and multinucleotide-polymorphism). 2023-12-22
bioconductor-chromheatmap public Heat map plotting by genome coordinate 2023-12-22
bioconductor-rsvsim public RSVSim: an R/Bioconductor package for the simulation of structural variations 2023-12-22
bioconductor-isomirs public Analyze isomiRs and miRNAs from small RNA-seq 2023-12-22
bioconductor-oppar public Outlier profile and pathway analysis in R 2023-12-22
bioconductor-coseq public Co-Expression Analysis of Sequencing Data 2023-12-22
bioconductor-translatome public Comparison between multiple levels of gene expression 2023-12-22
bioconductor-slalom public Factorial Latent Variable Modeling of Single-Cell RNA-Seq Data 2023-12-22
bioconductor-omicrexposome public Exposome and omic data associatin and integration analysis 2023-12-22
bioconductor-singscore public Rank-based single-sample gene set scoring method 2023-12-22
bioconductor-diffcoexp public Differential Co-expression Analysis 2023-12-22
bioconductor-doppelgangr public Identify likely duplicate samples from genomic or meta-data 2023-12-22
bioconductor-tissueenrich public Tissue-specific gene enrichment analysis 2023-12-22

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