Results for "Genome"

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  • Integrative Meta-Assembly Pipeline (IMAP): Chromosome-level genome assembler combining multiple de novo assemblies

    Chromosome-level genome assembler combining multiple de novo assemblies https://github.com/jkimlab/IMAP

    Tags: Integrative, Meta-Assembly, Pipeline, IMAP, Chromosome-level, genome, assembler, multiple, de novo, assemblies

    1701 days ago

  • ALF--a simulation framework for genome evolution.

    Artificial Life Framework (ALF) simulates a root genome into a number of related genomes. Result files include the resulting gene sequences, true tree and true MSAs. A description of ALF can be found in the following article: Daniel A Dalquen, Maria Anisimova, Gaston H Gonnet, Christophe Dessimo...

    Tags: ALF, simulation, framework, genome, evolution

    1649 days ago

  • simuG: a general-purpose genome simulator

    Simulated genomes with pre-defined and random genomic variants can be very useful for benchmarking genomic and bioinformatics analyses. Here we introduce simuG, a lightweight tool for simulating the full-spectrum of genomic variants (single nucleotide polymorphisms, Insertions/Deletions, copy num...

    Tags: simuG, general-purpose, genome, simulator

    1612 days ago

  • AirLift, a methodology and tool for comprehensively moving mappings and annotations from one genome to another similar genome

    We propose AirLift, a methodology and tool for comprehensively moving mappings and annotations from one genome to another similar genome while maintaining the accuracy of a full mapper.

    Tags: AirLift, methodology, tool, moving, mappings, annotations, genome, similar, genome

    1587 days ago

  • Shasta long read assembler

    The goal of the Shasta long read assembler is to rapidly produce accurate assembled sequence using as input DNA reads generated by Oxford Nanopore flow cells. Computational methods used by the Shasta assembler include: Using a run-length representation of the read sequence...

    Tags: Shasta, long, read, genome, assembler, tools, ngs

    1565 days ago

  • MitoZ: a toolkit for animal mitochondrial genome assembly, annotation and visualization

    MitoZ is a Python3-based toolkit which aims to automatically filter pair-end raw data (fastq files), assemble genome, search for mitogenome sequences from the genome assembly result, annotate mitogenome (genbank file as result), and mitogenome visualization. MitoZ is available from https://g...

    Tags: MitoZ, toolkit, animal, mitochondrial, genome, assembly, annotation, visualization, ngs, sequencing

    1555 days ago

  • mutatrix: a population genome simulator which generates simulated genomes.

    genome simulation across a population with zeta-distributed allele frequency, snps, insertions, deletions, and multi-nucleotide polymorphisms More at https://github.com/ekg/mutatrix ./mutatrix -S sample -P test/ -p 2 -n 10 reference.fasta

    Tags: mutatrix, population, genome, simulator, generates, simulated, genomes, ngs, test

    1551 days ago

  • HASLR: a tool for rapid genome assembly of long sequencing reads

    HASLR is a tool for rapid genome assembly of long sequencing reads. HASLR is a hybrid tool which means it requires long reads generated by Third Generation Sequencing technologies (such as PacBio or Oxford Nanopore) together with Next Generation Sequencing reads (such as Illumina) from the same s...

    Tags: HASLR, tool, rapid, genome, assembly, long, sequencing, reads

    1548 days ago

  • Biological databases !

    Now a days there are a lots of genomics databases available around the world. This bookmark is created to provide all links in one place ... ftp://ftp.ncbi.nih.gov/genomes/ https://hgdownload.soe.ucsc.edu/downloads.html

    Tags: download, database, ncbi, ftp, genome, dna, reads, genome, assembly, files, ucsc

    1536 days ago

  • SeqMule: Automated human exome/genome variants detection

    SeqMule takes single-end or paird-end FASTQ or BAM files, generates a script consisting of more than 10 popular alignment, analysis tools and runs the script line by line. Users can change the pipeline or fine-tune the parameters by modifying its configuration file.

    Tags: SeqMule, Automated, human, exome, genome, variants, detection

    1530 days ago