Alternatives and similar repositories for R-Tutorials

Users that are interested in R-Tutorials are comparing it to the libraries listed below

• NGSchoolEU / ngs19_python_intro
  Introduction to Python3
  ☆11Updated 4 years ago
• GenomicsUA / sc-school-2021
  ☆18Updated 4 years ago
• raqueeb / mlbook-titanic
  মেশিন লার্নিং: হাতে কলমে 'টাইটানিক 'প্রজেক্ট ওয়ার্কবুক
  ☆9Updated 5 years ago
• NGSchoolEU / ngs22
  Repository with NGSchool2022 materials
  ☆14Updated 2 years ago
• drtamermansour / nu-ngs01
  NGS-1 Data analysis course
  ☆37Updated 4 years ago
• SKawsar / Python_Fundamentals
  ☆13Updated 3 years ago
• QBangladesh / QBangladesh
  QCousin of QWorld. Bangladesh's first gateway to global quantum education.
  ☆14Updated last week
• ccbskillssem / snakemake_fa23
  CCB Skills Seminar (Fall 2023) - snakemake
  ☆15Updated last year
• saqifulalam / Basic-Intro-to-Analytics-and-ML-with-Python
  For those who have no previous coding background, and just starting to venture into Pyhton for analytics and some machine learning, this …
  ☆11Updated 2 years ago
• qtao / Genomic-Data-Science
  Genomic data science specialization
  ☆77Updated 9 years ago
• biosinodx / SCCNV
  SCCNV: a software tool for identifying copy number variation from single-cell whole-genome sequencing
  ☆12Updated 4 years ago
• raphaelmourad / CNN-for-genomics-training
  Training on CNN and basic ML for genomics
  ☆29Updated 4 months ago
• yufengwudcs / ScisTree
  Cell tree inference and genotype calling from noisy single cell data
  ☆9Updated 8 months ago
• KennethJHan / Genome-Analysis-Tutorial
  The Genome Analysis Tutorial Page.
  ☆13Updated 5 years ago
• bishwaG / Single-cell-RNA-seq-data-analysis-2018
  Event page: https://www.csc.fi/web/training/-/single-cell-rnaseq-r-2018
  ☆13Updated 6 years ago
• sib-swiss / NGS-variants-training
  GitHub for the SIB courses NGS - Genome variant analysis
  ☆25Updated 7 months ago
• sfu-compbio / PhISCS
  Tumor Phylogeny Reconstruction via Integrative use of Single Cell and Bulk Sequencing Data
  ☆11Updated 5 years ago
• rujinwang / SCOPE
  Single-cell COPy number Estimation
  ☆14Updated 2 years ago
• mkorshe / single_cell_transcritpomics_roadmap
  ☆17Updated 4 years ago
• lizamathews / CAISC
  CAISC (Clonal Architecture with Integrating SNV and CNV): a software to integrate copy number variation and single nucleotide mutations f…
  ☆12Updated 3 years ago
• YJulyXing / SECNVs
  A tool for simulating CNVs for WES data. It simulates rearranged genome(s), short reads (fastq) and BAM file(s) automatically in one sing…
  ☆17Updated 5 years ago
• annalam / cfdna-wgs-manuscript-code
  Code used to generate the results in "Somatic chronology of treatment-resistant prostate cancer via deep whole-genome ctDNA sequencing"
  ☆14Updated last year
• ngs-docs / 2016-adv-begin-shell-genomics
  Workshop content for http://dib-training.readthedocs.org/en/pub/2016-01-13-adv-beg-shell.html
  ☆12Updated 7 years ago
• AlexandrovLab / EnsembleVariantCallingPipeline
  The EnsembleVariantCallingPipeline takes files in FASTQ or BAM format and performs SNV and INDEL variant calling from 4 variant callers (…
  ☆13Updated 2 years ago
• crazyhottommy / ML-YouTube-Courses
  📺 Discover the latest machine learning / AI courses on YouTube.
  ☆22Updated last year
• cbg-ethz / COMPASS
  ☆23Updated 10 months ago
• crazyhottommy / compbio_resources_chatomics
  ☆27Updated 2 years ago
• mbourgey / EBI_cancer_workshop_SNV
  ☆15Updated 3 years ago
• GuanLab / FastClone_GuanLab
  ☆15Updated 3 years ago
• faridrashidi / trisicell
  Scalable tumor phylogeny inference and validation from single-cell RNA or DNA data
  ☆14Updated last year