Courses – BioCode

Hands-on ATAC-Seq Data Analysis for Identification of Chromatin Accessibility Using Linux & R

Hands-on ATAC-Seq Data Analysis for Identification of Chromatin Accessibility Using Linux & R

By BioCode Team In ATAC-Seq, Linux

Summer Research Program on Single-Cell RNA-Seq

5.00

(1)

Summer Research Program on Single-Cell RNA-Seq

3h 57m

By BioCode Team In Single Cell, Summer Research Program, Workshops

Summer Research Program

5.00

(1)

Summer Research Program

9h 39m

By BioCode Team In Summer Research Program

Basic Membership

5.00

(1)

Basic Membership

50h 20m

By BioCode Team In Bioinformatics Programming, In-Depth

/ month

Introduction to Bioinformatics & Its Advancements

4.75

(68)

Introduction to Bioinformatics & Its Advancements

3h 26m

By BioCode Team In Beginner's, Free

All-Access ruby plan

All-Access ruby plan

125h 34m

By BioCode Team In Computational Drug & Vaccine Discovery, Immunology, Linux, Molecular Biology, NGS, Python, R, RNA-Seq, Vaccine Discovery

/ year

Workshop Cancer Therapeutics & Computational Drug Discovery

3.00

(1)

Workshop Cancer Therapeutics & Computational Drug Discovery

By BioCode Team In Cancer therapeutics, Hands-on, Workshops

End-to-End RNA-Seq Data Analysis With Python-Based Pipeline

End-to-End RNA-Seq Data Analysis With Python-Based Pipeline

7h

By BioCode Team In NGS, Python, RNA-Seq

Cancer Genomics: NGS (Whole Genome Sequencing) Variant Calling Using Linux

Cancer Genomics: NGS (Whole Genome Sequencing) Variant Calling Using Linux

11h 24m

By BioCode Team In Cancer Genomics, Linux, NGS, WGS

Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Python

Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Python

By BioCode Team In NGS, Python

Cancer Genomics: NGS (Whole Exome Sequencing) Variant Calling Using Linux

Cancer Genomics: NGS (Whole Exome Sequencing) Variant Calling Using Linux

By BioCode Team In Cancer Genomics, Linux, NGS, WES

Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Linux

Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Linux

By BioCode Team In Linux, NGS

Hands-on: Single-Cell RNA-Sequencing Data Analysis Using Python [Complete Training]

Hands-on: Single-Cell RNA-Sequencing Data Analysis Using Python [Complete Training]

By BioCode Team In Python, RNA-Seq, Single Cell

Hands-on: Single-Cell RNA-Sequencing Data Analysis Using Command-Line and R [Complete Training]

4.67

(3)

Hands-on: Single-Cell RNA-Sequencing Data Analysis Using Command-Line and R [Complete Training]

10h 24m

By BioCode Team In R, RNA-Seq, Single Cell

Exploratory Data Analysis (EDA) in Python for Machine Learning in Bioinformatics

Exploratory Data Analysis (EDA) in Python for Machine Learning in Bioinformatics

3h 43m

By BioCode Team In Machine Learning, Python

Introduction to Anaconda and Jupyter-Notebook for Bioinformatics

Introduction to Anaconda and Jupyter-Notebook for Bioinformatics

49m

By BioCode Team In Machine Learning

PyMol MasterClass: Perform Expert Level 3D Structure Visualization for Drug Discovery

2.00

(1)

PyMol MasterClass: Perform Expert Level 3D Structure Visualization for Drug Discovery

1h 8m

By BioCode Team In drug discovery

Hands-on: NGS (Whole Genome Sequencing) Variant Calling for Microbial Genomics

Hands-on: NGS (Whole Genome Sequencing) Variant Calling for Microbial Genomics

5h 37m

By BioCode Team In NGS

Machine Learning Series: Manipulation of Biological Datasets in R using Dplyr and TidyR

3.00

(2)

Machine Learning Series: Manipulation of Biological Datasets in R using Dplyr and TidyR

By BioCode Team In Machine Learning

All-Access Membership

5.00

(2)

All-Access Membership

72h 54m

By BioCode Team In Computational Drug & Vaccine Discovery, Immunology, Linux, Molecular Biology, NGS, Python, R, RNA-Seq, Vaccine Discovery

/ month