Alternatives and similar repositories for Numerical-Methods:

Users that are interested in Numerical-Methods are comparing it to the libraries listed below

• anuj-das-10 / DS-Algorithms-Practicals
  Implementation of Data Structures and Algorithms using C/C++ Programming Languages.
  ☆10Updated 3 years ago
• anuj-das-10 / Internet-Technologies
  This Repository contains solution of all the Internet Technologies practical questions.
  ☆11Updated 2 years ago
• anuj-das-10 / Network-Programming
  This Repository contains solution of all the Network Programming practical questions.
  ☆19Updated 2 years ago
• anuj-das-10 / Programming-Fundamentals-using-C-CPP
  This Repository contains solution of all the C/C++ practical questions.
  ☆16Updated 2 years ago
• anuj-das-10 / Programming-in-JAVA
  This Repository contains solution of all the JAVA practical questions.
  ☆13Updated 2 years ago
• gcc-x-csd / GCCxCSD
  2023 Final Semester Web Project by @anuj-das-10, @Kaustav-Purkayastha & @Debojyoti-hash
  ☆18Updated last year
• PacificBiosciences / pb-CpG-tools
  Collection of tools for the analysis of CpG data
  ☆80Updated 2 months ago
• marbl / Winnowmap
  Long read / genome alignment software
  ☆284Updated 5 months ago
• GregoryFaust / samblaster
  samblaster: a tool to mark duplicates and extract discordant and split reads from sam files.
  ☆231Updated 3 years ago
• AstraZeneca-NGS / VarDict
  VarDict
  ☆198Updated last year
• Illumina / DRAGMAP
  DRAGEN open-source mapper
  ☆171Updated last year
• trinityrnaseq / RNASeq_Trinity_Tuxedo_Workshop
  materials for the RNA-Seq workshop on Trinity and Tuxedo, covering de novo and genome-guided transcript assembly and downstream analysis.
  ☆48Updated 8 years ago
• arq5x / lumpy-sv
  lumpy: a general probabilistic framework for structural variant discovery
  ☆324Updated 2 years ago
• PacificBiosciences / FALCON
  FALCON: experimental PacBio diploid assembler -- Out-of-date -- Please use a binary release: https://github.com/PacificBiosciences/FALCON…
  ☆205Updated 3 years ago
• waldronlab / BugSigDBcuration
  For documenting issues related to BugSigDB curation.
  ☆14Updated 3 weeks ago
• jts / sga
  de novo sequence assembler using string graphs
  ☆241Updated 5 years ago
• dnanexus-archive / parliament2
  Runs a combination of tools to generate structural variant calls on whole-genome sequencing data
  ☆101Updated 4 years ago
• gt1 / biobambam2
  Tools for early stage alignment file processing
  ☆93Updated 6 years ago
• lh3 / CHM-eval
  ☆54Updated 4 years ago
• adamewing / bamsurgeon
  tools for adding mutations to existing .bam files, used for testing mutation callers
  ☆240Updated 6 months ago
• walaj / svaba
  Structural variation and indel detection by local assembly
  ☆245Updated last month
• timkahlke / LongRead_tutorials
  Workflows and tutorials for LongRead analysis with specific focus on Oxford Nanopore data
  ☆137Updated 3 years ago
• TreesLab / NCLscan
  We have developed a new pipeline, NCLscan, which is rather advantageous in the identification of both intragenic and intergenic "non-co-l…
  ☆6Updated last year
• cancerit / BRASS
  Breakpoints via assembly - Identifies breaks and attempts to assemble rearrangements in whole genome sequencing data.
  ☆57Updated 9 months ago
• RemiAllio / MitoFinder
  MitoFinder: efficient automated large-scale extraction of mitogenomic data from high throughput sequencing data
  ☆102Updated last year
• GoekeLab / awesome-nanopore
  A curated list of awesome nanopore analysis tools.
  ☆263Updated 8 months ago
• mahulchak / quickmerge
  A simple and fast metassembler and assembly gap filler designed for long molecule based assemblies.
  ☆206Updated 2 years ago
• arq5x / poretools
  a toolkit for working with Oxford nanopore data
  ☆242Updated 2 years ago
• KolmogorovLab / Severus
  A tool for somatic structural variant calling using long reads
  ☆128Updated 2 weeks ago
• NCBI-Hackathons / TheHumanPangenome
  A Strategy for Building and Using a Human Reference Pangenome
  ☆70Updated 4 years ago