Analysis Driven by
Best-Published Pipelines
My Services
RNA sequencing analysis
RNA sequencing analysis for data obtained from organisms with a reference genome and annotation.
Variant calling
Identify germline or somatic short variants (SNPs and Indels) in your samples to further produce a multi-VCF format.
(https://gatk.broadinstitute.org/hc/en-us/sections/360007226651-Best-Practices-Workflows)
Single-cell analysis
Identify and interpret heterogeneity from single-cell RNA-seq data and integrate diverse types of single-cell data.
Assembly
Assemble viral or bacterial genomes from long or short reads.
Enrichment analysis
Enrichment Analysis for Uncovering Gene Function Networks
(clusterProfiler 4.0: A universal enrichment tool for interpreting omics data. doi: 10.1016/j.xinn.2021.100141)
Methylation sequencing analysis
High-resolution methylation sequencing analysis for epigenetic insights
(The nf-core framework for community-curated bioinformatics pipelines https://zenodo.org/record/8029942)
ChipSeq analysis
Enrichment Analysis for Uncovering Gene Function Networks
(ChIP-AP: an integrated analysis pipeline for unbiased ChIP-seq analysis https://doi.org/10.1093/bib/bbab537)
Personalized Analysis
A custom analysis that matches your expertise according to the latest research. The pipeline will be based on previously published findings.
There's no extra charge for its development.