Browse data: Bioinformatics application

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; Adapter removal Assembly Base-calling Bisulfite mapping Comparative genomics Conversion DNA barcoding De-novo assembly Differential Binding Haplotype inference Hidden Markov Model Local sequence alignment Mapping Methylation calling Modelling and simulation Nucleic acid sequence feature detection Peak calling Quality assessement Quality control RRNA filtering Read alignment Read mapping Read pre-processing Read summarisation Sequence alignment Sequence alignment visualisation Sequence analysis Sequence annotation Sequence assembly Sequence contamination filtering Sequence error correction Sequence parsing Sequence redundancy removal Sequence trimming Sequencing quality control Split-read mapping Standardisation and normalisation Statistical calculation Visualisation Whole genome breakend assembly

; Cancer biology ChIP-seq Community analysis Comparative genomics Copy number estimation DNA methylation Epigenetics Epigenomics Exome Exome analysis Exome and whole genome variant detection Exome capture Gene structure Genetic variation analysis Genomics High-throughput sequencing Indel detection Mapping Metagenomics Next Generation Sequencing Personalised medicine Phylogenetics Protein structure analysis Quality control RNA-Seq RNA-Seq alignment Rarefaction Regulatory genomics Resequencing SNP detection Sequence alignment Sequence analysis Sequence assembly Sequence assembly (de-novo assembly) Sequence assembly (de novo assembly) Sequencing Structural variation Transcription factors and regulatory sites Transcriptome assembly Transcriptomics Whole genome resequencing