Next Generation Sequencing (NGS) has revolutionized the way that we address complex biological questions. As sequencing output rapidly increases and experimental scales get bigger, library preparation becomes one of the major bottlenecks for NGS. This course provides a comprehensive hands-on…
- Home
- Getting Started
- Services
- Short-Read Sequencing Services – Illumina & Element Bio AVITI
- DNA Sequencing (whole-genome shotgun, targeted, amplicon, exome, ChIP, reduced-representation, Methyl, …)
- RNA-Sequencing (high-throughput mRNA-Seq, total RNA-seq, 3′-Tag-Seq, miRNA-seq, … )
- Gene Expression Profiling with 3′-Tag-Seq
- PacBio Revio Library Prep & Sequencing
- Nanopore Sequencing – PromethION
- Linked Read Sequencing – 10X Genomics Chromium Technology
- High Molecular Weight DNA Isolation (HMW-DNA)
- Sample and Library Requirements Tables
- DNA/RNA Quantification & Library QC
- DNA and RNA Extraction at the Taqman Core
- Single Cell Expression Profiling & Genomics (10X Genomics, Parse Biosciences, and Plate-based scRNA-Seq)
- Spatial Transcriptomics
- Genotyping – Illumina Infinium, Fluidigm EP1
- Consultations
- Bioinformatics –>
- Sample Submission & Forms
- Prices
- FAQ
- Shared Equipment
- Booking Shared Instruments – Equipment Calendar
- Equipment Training & Use
- Agilent Bioanalyzer 2100
- FilterMax F5 Plate Reader
- Qubit Fluorometer
- Caliper LabChip GX (high-throughput Bioanalyzer)
- Nanodrop Spectrophotometer
- Sonicators
- BluePippin and PippinHT
- Robotic Liquid Handlers
- Fluidigm C1 – Single Cell Genomics
- Fluidigm Access Array
- Equipment Calendar
- News & Workshops
- Accounts & Calendars
- Contact
