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Bioinformatics for Everyone Beginner to Expert Guide 2023

سرفصل های دوره

Bioinformatics Beginners to advance course to learn in 10 hours to understand the simple and complex topics of bioinfo


1 - Introduction of Bioinformatics
  • 1 - Introduction
  • 2 - Introduction of Bioinformatics field
  • 3 - History of bioinformatics
  • 4 - Components of bioinformatics
  • 5 - Working in Bioinformatics
  • 6 - Career Outlook for bioinformaticians
  • 7 - Careers for bioinformaticians
  • 8 - Applications of Bioinformatics
  • 9 - Applications of Bioinformatics Pt2

  • 2 - Biological Databases
  • 10 - Introduction of Biological Databases
  • 11 - Types of Biological Databases
  • 12 - Difference Between Primary and Secondary Databases
  • 13 - Primary Databases
  • 14 - Explaining Primary Databases
  • 15 - Explaining Primary Databases pt2
  • 16 - Explaining Primary Databases Last Part
  • 17 - Introduction of Secondary Databases
  • 18 - Explaining Secondary Databases
  • 19 - Explaining Secondary Databases pt2
  • 20 - Explaining Secondary Databases Pt3
  • 21 - Explaining Secondary Databases Pt4
  • 22 - Introduction of Literature Databases
  • 23 - Explaining Literature Databases

  • 3 - File Formats in Bioinformatics
  • 24 - Introduction of File Formats
  • 25 - Explaining different File Formats
  • 26 - Summary of File Formats

  • 4 - Segment 3 Sequence Alignment and Tools
  • 27 - Introduction of Sequence Alignment
  • 28 - History of Sequence Alignment
  • 29 - Alignment Methods
  • 30 - Interpretation of Sequence Alignment
  • 31 - Representation and Storing of Sequences
  • 32 - Significance and Uses of Sequence Alignment
  • 33 - Software Used for Sequence Alignment
  • 34 - Pairwise Sequence Alignment
  • 35 - Tools for Pairwise Sequence Alignment
  • 36 - Multiple Sequence Alignment
  • 37 - Tools for Multiple Sequence Alignment
  • 38 - Clustal tool for alignment

  • 5 - Command line bioinformatics
  • 39 - Introduction and Why CLI in Bioinformatics
  • 40 - CLI and GUI Explanation
  • 41 - if we already have Graphical user interface system why we should use CLI
  • 42 - Short Practical with Programming Language
  • 43 - Why Would You Use CLI over GUI
  • 44 - Foundation behind CLI Shell explanation
  • 45 - Drawbacks of CLI and GUI
  • 46 - Linux Introduction and Usage Over years
  • 47 - Linux Distros
  • 48 - Why Ubuntu Operating System
  • 49 - WSL Explanation
  • 50 - Linux Vs Unix
  • 51 - Practical Making A Subsystem For Linux In Windows OS
  • 52 - Linux File Handling Commands
  • 53 - Accessing And Creating Files In Windows Os
  • 54 - Basic Process Management Commands for Linux OS
  • 55 - Eutilities on the Linux Command Line
  • 56 - Installing NCBI through CLi
  • 57 - Entrez Direct Functions
  • 58 - Mrna And Protein Seq Retrieval
  • 59 - Batch Retrieval of Protein Using Taxon Id
  • 60 - Retrieving CDS From Reference Genome
  • 61 - Explaining Different Commands

  • 6 - Bioinformatics and Genomics on GUI
  • 62 - Introduction of Course Section
  • 63 - Nextgeneration sequencing
  • 64 - Generations of Sequencing
  • 65 - NGS Workflow
  • 66 - SRA Database introduction
  • 67 - SRA File
  • 68 - Galaxy Server Intro to Goals
  • 69 - Galaxy Server And Objects
  • 70 - Getting Onto Galaxy
  • 71 - Tools For NGS Data Analysis
  • 72 - Getting SRA Runs from Databases And platform
  • 73 - Ncbi Genome to Galaxy
  • 74 - Getting Sra Runs To Galaxy
  • 75 - Fastqc Tool To Dataset Generated Dataset
  • 76 - Trimmomatic Tool On Dataset
  • 77 - Alignmentgenome Mapping
  • 78 - Abundance Estimation Tool On Dataset
  • 79 - From Values To Visuals Heatmap

  • 7 - Bioinformatics and Genomics on CLI
  • 80 - NGS Understanding
  • 81 - Getting the SRA Reads
  • 82 - Bioinformatics Pipeline
  • 83 - Checking the Quality of Data
  • 84 - Quality Trimming of data
  • 85 - Aligners and Aligning Reads to genome
  • 86 - SAM and Bam File Indexing and Sorting
  • 87 - Feature Extraction
  • 88 - Pipeline Code.html

  • 8 - Variant Calling on Command line
  • 89 - Introduction of Course Section
  • 90 - Variants and Types
  • 91 - Understanding the Metadata and Softwares
  • 92 - Getting Data From SRA Using SRA Toolkit
  • 93 - Quality Control and Trimming
  • 94 - Sam and Bcf Tools and Fixing NS and Calling Variants
  • 95 - Alignment to Reference Genome
  • 96 - Separation of SNPs and Indels Variants
  • 97 - Visualizing Variants Using IGV and UCSC Browser
  • 98 - Pipeline Code.html

  • 9 - Bioinformatics And Proteomics
  • 99 - Section Introduction
  • 100 - Explaining Homology Modeling
  • 101 - GUI based Modeling of Proteins
  • 102 - Command Line based Protein Modeling
  • 103 - DeNovo and Machine Learning Methods
  • 104 - Phylogenetics Analysis
  • 105 - Motifs and Domains analysis
  • 106 - Protein Physical Parameters and Location Analysis
  • 107 - ProteinProtein Interaction and Enrichment Analysis
  • 108 - Proteins Pathway Analysis
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    تاریخ انتشار: 10 فروردین 1402
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