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Bioinformatics Hub
🧪 Interactive Next-Gen Learning Platforms

Master Modern Bioinformatics Workflows

Hands-on interactive simulators, command builders, and reproducible pipelines for Genomics, Transcriptomics, Proteomics, and Microbiome Data Science.

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Coming Soon
Genomics • Alignment Utilities

SAMtools & BAMtools Suite

Master high-throughput sequence alignment manipulation: view, sort, index, filter, and flagstat BAM/CRAM files. Interactive bitwise flag decoder and depth coverage analyzer.

  • SAM / BAM / CRAM Conversion
  • Bitwise Flag Decoders
  • Coverage Depth Analysis
  • Variant Calling (mpileup)
Coming Soon
Transcriptomics • Splice-Aware Alignment

HISAT2 RNA-Seq Alignment

Fast and sensitive splice-aware alignment of RNA-seq reads using Hierarchical Graph FM Indexing. Comprehensive exon-intron junction models and transcriptome indexing.

  • Splice-Aware Mapping
  • Genome Indexing (HGFM)
  • Stranded RNA-Seq
  • Junction Detection
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Coming Soon
Genomics • Short Read Alignment

Bowtie & Bowtie 2

Ultrafast and memory-efficient alignment of sequencing reads to long reference genomes using Burrows-Wheeler Transform. Optimized for gDNA, ChIP-seq, and ATAC-seq workflows.

  • BWT Indexing
  • End-to-End vs Local Alignments
  • ChIP-seq / ATAC-seq
  • Multi-mapping Read Handling
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Coming Soon
Transcriptomics • Gene Expression

DESeq2 & EdgeR Workbench

End-to-end RNA-Seq differential expression analysis: raw count normalization, variance-stabilizing transformation, dispersion estimation, PCA visualizations, and volcano plots.

  • Count Normalization
  • Negative Binomial GLMs
  • Volcano & Heatmap Plots
  • Batch Effect Correction
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Coming Soon
Proteomics • Mass Spectrometry

MaxQuant & MSFragger Lab

Liquid chromatography-mass spectrometry (LC-MS/MS) data science: peptide-spectrum matching, label-free quantification (LFQ), TMT isobaric labeling, and protein network analysis.

  • DDA & DIA Analysis
  • MaxLFQ & TMT Quant
  • Post-Translational Mod (PTMs)
  • STRING / Cytoscape Pathways
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Coming Soon
Genomics • Variant Discovery

GATK Best Practices Pipeline

Standardized pipeline for germline and somatic variant discovery: base quality score recalibration (BQSR), HaplotypeCaller, VCF filtering, and functional annotation with SnpEff / ANNOVAR.

  • SNV & Indel Discovery
  • BQSR Recalibration
  • Joint Genotyping
  • VCF Filtering & Annotation
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Coming Soon
Metagenomics • Shotgun Assembly

Shotgun Assembly & MAG Binning

Reconstruct Metagenome-Assembled Genomes (MAGs) from complex environmental samples using MEGAHIT, SPAdes, MetaBAT2, CheckM quality assessment, and GTDB-Tk phylogenomic taxonomy.

  • De Novo Metagenome Assembly
  • Tetranucleotide Binning
  • CheckM Completeness & Contam
  • GTDB-Tk Phylogenetics
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Coming Soon
Proteomics • Structural Biology

AlphaFold & ColabFold Modeling

Predict 3D macromolecular structures from amino acid sequences using AI models. Evaluate per-residue confidence (pLDDT), Predicted Aligned Error (PAE), and multimer protein-protein docking.

  • AlphaFold2 / AlphaFold3
  • pLDDT & PAE Interpretation
  • Protein-Protein Interfaces
  • PyMOL / ChimeraX Scripts
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Coming Soon
Metagenomics • Taxonomic Profiling

Kraken 2 & Bracken Profiler

Ultra-fast k-mer classification and abundance re-estimation for whole-genome shotgun metagenomics. Build custom databases and estimate true species-level relative abundances.

  • Exact k-mer Taxonomic Labeling
  • Bracken Bayesian Re-estimation
  • Custom Database Generation
  • Krona / Pavian Visualizations