Be default we will demultiplex all sequencing data from libraries generated by our facility as well as from customer libraries with barcodes sequenced in separate indexing reads (e.g. using Truseq-style adapters). This is in contrast to adapters with old style in-line…
- 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
- 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
