717 results found for "DNA sequencing"
Targeted Sequencing
Efficiently scale your targeted next-generation sequencing (NGS) library preparation with the Juno™ and Access Array™ systems. Process more samples per batch than with other methods, reduce hands-on time and handling error, drive down reagent and operating costs and customize a targeted DNA panel to serve your specific application.
Learn more about: Juno Access Array
Learn more about reagents for targeted sequencing.
Support for: Juno Access Array
More search results:
-
product insert
C1 Reagent Kit for DNA Sequencing Product Insert
This kit provides the necessary reagents to support single-cell capture and amplification of genomic DNA from single cells.
-
faq
What do I need to perform targeted DNA sequencing library preparation?
Required: Advanta™ NGS Library Prep Reagent Kit/Bundle (101-7663, 101-7666, 101-7667, 101-7669), Targeted DNA Seq Primer Pools (ASY-MPX-XS, ASY-MPX-S, ASY-MPX-M, ASY-MPX-L), Targeted DNA Seq Barcode Plates (101-0744), IFCs, Barrier Tape, and Control Line Fluid. …
-
media
Striving for a Cancer Cure, One Cell at a Time
McGill’s Jiannis Ragoussis shares breakthrough single-cell DNA sequencing research …
-
faq
What is the minimum DNA input for assays using the Advanta NGS Library Prep Reagent Kit?
100 ng input per sample for human genomic DNA or for DNA of equivalent genome size. For larger genomes, contact Fluidigm support (fluidigm.com/contacts) for guidance on input requirements. …
-
Poster
Single-Cell Analysis of Breast Cancer Single Nucleotide Variants
The DNA Seq protocol on the C1 System generates whole genome amplified DNA suitable for targeted resequencing, whole exome sequencing, and whole genome sequencing from up to 96 individual cells in a single workflow.
-
faq
Which sequencing systems are compatible with the Advanta NGS Library Prep Reagent Kit?
The Advanta™ NGS Library Prep Reagent Kit is designed to prepare libraries for sequencing on Illumina®, MiniSeq™, MiSeq™, NextSeq™, and HiSeq® systems. …
-
Infographic
The Search for the Hidden Mutation, One Cell at a Time
This Fluidigm infographic shows how somatic mutations cause disease, including how single-cell DNA sequencing can reveal hidden mutations in cell populations.
-
Protocol
C1 System for DNA Sequencing Protocol
version I1
-
article
The Single-Cell Analysis Technologist
Burroughs Wellcome Fund honors Charles Gawad’s genomics mission for pediatric biology …
-
faq
Targeted DNA Sequencing Library Prep with Juno: FAQs
Frequently Asked Questions about targeted DNA sequencing library preparation with Juno.
-
data sheet
Targeted DNA Sequencing Library Prep with Juno: FAQs
Frequently Asked Questions about targeted DNA sequencing library preparation with Juno.
-
article
-
system
Juno
Targeted NGS library preparation, gene expression and genotyping …
-
brochure
-
consumable
Advanta Assays and Kits
Combining microfluidics technology with optimized reagents produces high-quality results in less time. …
-
resource
C1 System Software
The C1™ system supports DNA sequencing, mRNA sequencing, targeted gene expression, miRNA analysis and additional applications through the C1 Open App™ IFC (integrated fluidic circuit). Download the C1 system software update and then follow the instructions for updating the C1 system software.
… -
resource
Script Hub
Script Hub™ is your central source for C1™ methods and applications. Get access to scripts and other applications developed by Fluidigm and the C1 community, including epigenetics, mRNA sequencing, DNA sequencing, cell staining and more.
… -
faq
What materials are included in each kit?
Each Advanta™ CFTR NGS Library Prep Assay contains targeted DNA sequencing library reagents (including 4X Master Mix, DNA polymerase and adapter mix), CFTR primers, IFCs and Control Line Fluid. …
-
brochure
Access Array Sequencing
From sample to sequence, ready for next-generation sequencing
-
system
Access Array
A modular, flexible targeted DNA sequencing library preparation system …