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Advanced Epigenetics Sequencing
- Assay for Transposase Accessible Chromatin with high-throughput sequencing
- Genome-wide Chromatin Conformation Capture method using proximity ligation
- Low Input Whole-Genome BiSulfite Sequencing
- Reduced Representation Bisulfite Sequencing
- Whole Genome Oxidative BiSulfite Sequencing
Challenging DNA Sequencing
- Formalin-Fixed Paraffin-Embedded Exome Sequencing
- Formalin-fixed paraffin-embedded RNA Sequencing
- Ultra Low ancient DNA Sequencing
- Ultra Low DNA Sequencing
Immunogenomics
- Antibody Sequencing
- B Cell Receptor Sequencing
- Human Leukocyte Antigen Sequencing
- T Cell Receptor Sequencing
In situ Sequencing
- Barcode sequencing and imaging
- generating Rolling Circle Amplification products in the tissues
- Spatial RNA Sequencing
Integrative Data Analysis
- Bioinformatic secondary analysis
Long Read Sequencing
- 16S ribosomal RNA Sequencing
- Chromium Based Sequencing (scaffolding)
- Mate Pair Sequencing
- Nanopore Sequencing
- PacBio sequencing
Single cell Sequencing
- Single Cell ATAC Sequencing
- Single Cell DNA Sequencing
- Singel Cell DNA and RNA Sequencing
- Single Cell multiome Sequencing
- Single Cell RNA and V(D)J Sequencing
- Single Cell RNA Sequencing
- Single Cell T Cell Receptor Sequencing
High-throughput NGS technologies
- RNA sequencing (RNA-Seq) uses next-generation sequencing (NGS) to measure the presence and quantity of RNA (cellular transcriptome) in a biological sample at a given moment.
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- Whole-exome sequencing (WES), is a genomic technique for sequencing all of the protein-coding regions of genes in a genome.
- Whole-genome sequencing (WGS) is a comprehensive method for analyzing entire genomes.
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