Results for "Study"

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  • Bioinformatics Scripts

    Some of the useful bioinformatics scripts. For example ... contig-stats.pl is a Perl script that will automatically describe features of a sequence assembly. http://milkweedgenome.org/?q=scripts

    Tags: Bioinformatics, Computational Biology, Education, Study, Script, Perl, Python

    3351 days ago

  • BioScripts

    You are requested to please bookmark collection of bioinformatics tools, scripts, codes that can be pieced together in a very easy and flexible manner to perform both simple and complex bioinformatics tasks. The next-generation sequencing included whole genome sequencing(WGS), transcriptome sequ...

    Tags: Bioinformatics, Computational Biology, Education, Solution, Study, Script, Perl, Python, R, Code

    3224 days ago

  • Bioinformatics Made Easy Search: Bioinformatics tools and run genomic analysis in the cloud

    InsideDNA makes hundreds of bioinformatics tools immediately available to run via an easy-to-use web interface and allows an accurate search across all functions, tools and pipelines. With InsideDNA, you can upload and store your own genomic/genetic datasets in a limitless cloud space, and insta...

    Tags: Bioinformatics, Computational Biology, Education, Solution, Puzzle, Study, Script, Cloud, Server, Work, InsideDNA

    3172 days ago

  • Pattern Searching in a Single Genome

    Pattern searching holds much importance for biologists , for the understanding of DNA ( and its functionality) can be more than a matter of satisfying curiosity , but also give answers to many issuess uchas medical conditions . However,there are a number of ways of searching with in a single chro...

    Tags: Bioinformatics, Genomics, Pattern, Chromosome, Study

    2972 days ago

  • SEX-DETector: A Probabilistic Approach to Study Sex Chromosomes in Non-Model Organisms

    SEX-DETector is a probabilistic method that relies on RNAseq data from a cross (parents and progeny of each sex) to infer autosomal and sex-linked genes (genes located on the non recombining part of sex chromosomes). How does SEX-DETector work? SEX-DETector does not require prior sequencing of ...

    Tags: SEX-DETector, Probabilistic, Approach, Study, Sex, Chromosomes, Non-Model, Organisms

    2157 days ago

  • Choosing the Right NGS Sequencing Instrument for Your Study

    The right sequencing instrument for your study depends on your project goal. Setting aside turnaround time and price, it essentially comes down to the numbers of reads and read length you need for your experiment. Below, we've described and compared metrics for each of the instruments available. ...

    Tags: Choose, NGS, Sequencing, Instrument, Study

    681 days ago

  • EWAS: epigenome-wide association study software 2.0

    EWAS2.0 can analyze EWAS data and identify the association between epigenetic variations and disease/phenotype. On the basis of EWAS1.0, we have added more distinctive features. EWAS2.0 software was developed based on our “population epigenetic framework” and can perform: (1) epigenom...

    Tags: EWAS, epigenome-wide, association, study, software

    2227 days ago

  • Mulan: Multiple-sequence local alignment and visualization for studying function and evolution

    Mulan: Multiple-sequence local alignment and visualization for studying function and evolution Mulan (http://mulan.dcode.org/), a novel method and a network server for comparing multiple draft and finished-quality sequences to identify functional elements conserved over evolutionary time. Mulan ...

    Tags: Mulan, Multiple-sequence, local, alignment, visualization, study, function, evolution

    2071 days ago

  • Coronavirus Resources !

    2019nCoVR features comprehensive integration of genomic and proteomic sequences as well as their metadata information from the GISAID, NCBI, NMDC and CNCB/NGDC. It also incorporates a wide range of relevant information including scientific literatures, news, and popular articles for science disse...

    Tags: Corona, virus, China, Resources, CoVID, covid, china, genome, assembly, dna, rna, sequences, evolution, study, comparative, genomics

    1449 days ago

  • PheWAS: R package is designed to provide an accessible interface to the phenome wide association study

    The PheWAS R package is designed to provide an accessible interface to the phenome wide association study. For a description of the methods available and some simple examples, please see the package vignette or the R documentation. For installation help, see below. ##Installing the PheW...

    Tags: PheWAS, R, package, accessible, interface, phenome, wide, association, study

    1365 days ago