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NGS Overview Digital Brochure Feb26 2018 No Crops

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0% found this document useful (0 votes)
55 views6 pages

NGS Overview Digital Brochure Feb26 2018 No Crops

Alat sekuensing canggih

Uploaded by

ipan
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Next Generation Sequencing

RNA
Sequencing
Next-Generation RN
Sequencing

Quality
Cancer Panels Targeted Resequencing
& Cancer Panels
Metagenomics
Sequencing
FuzeSeq Antibody
Sequencing
Adventitious Agent
Contamination Testing
Bioinformatics
Solutions
Amplicon
Sequencing
Amplicon
Sequencing
ChIP-Se

RNA-Seq
Speed
Small RNA-Seq Exome Sequencing Standalone NGS Services Cancer Panels Targeted Resequencing
& Cancer Panels
Metagenomics FuzeSeq Antibody
Sequencing
Adventitious Agent Bioinformatics Amplicon ChIP-Seq Whole Genome
Whole Genome
OncoGxOne

Value
Sequencing Contamination Testing Solutions Sequencing Sequencing

Sequencing

Service
Next-Generation
Sequencing
RNA-Seq Small RNA-Seq Exome Sequencing Standalone NGS Services Cancer Panels
Targeted
Targeted Resequencing
Resequencing
& Cancer Panels
Meta
Seq

Metagenomics
eneration RNA-Seq Small RNA-Seq Exome Sequencing Standalone NGS Services Cancer Panels Targeted Resequencing Metagenomics FuzeSeq
encing & Cancer Panels Sequencing Seque

Exome
Sequencing
Next-Generation RNA-Seq Small RNA-Seq Exome Sequencing Standa
Sequencing

ChIP
els Targeted Resequencing Metagenomics FuzeSeq Antibody Adventitious Agent Bioinformatics Amplicon Sequencing
ChIP-Seq Whole Ge
& Cancer Panels Sequencing Sequencing Contamination Testing Solutions Sequencing Sequen

Sequencing
Next-Generation RNA-Seq Small RNA-Seq Exome Sequencing
Only
Standalone NGS Services Cancer
Sequencing
EXPERIENCE THE GENEWIZ DIFFERENCE
Industry-leading Turnaround Time Exceptional Data Quality
EXTRACTION LIBRARY
>98% projects delivered PREP
on-time SEQUENCING BIOINFORMATICS
Far exceeds manufacturer’s
with extraordinarily fast turnaround criteria with >90% bases scoring
time options Q30 or better (most applications)

Optimized Workflows
Automated
Latest Wide
platforms with Range of
automated
 Highest Customer Satisfaction
Latest Platforms/ Customizable
Referrals from existing
Processes Libraries Offered Technology Offerings
processes increase scalability, improve customers are the #1 source of
reproducibility, and reduce costs new GENEWIZ customers

EXTRACTION LIBRARY PREP SEQUENCING BIOINFORMATICS

users Dedicated Project Managers


Expert study managers provide support
throughout the project

Automated Wide Range of Latest Platforms/ Customizable


Processes Libraries Offered Technology Offerings

QUALITY THROUGH
QUALITY THROUGH EVERY
EVERYSTEP
STEP

EXTRACTION LIBRARY PREP SEQUENCING BIOINFORMATICS

Automated Wide Range of Latest Platforms/ Customizable


Processes Libraries Offered Technology Offerings
NEW AND PROPRIETARY SERVICES
Amplicon-EZ
Fast, ultra-deep sequencing of pre-made PCR products.
Starting at $50/sample with results in as few as 3 business days.

ormatics Amplicon 16S MetaVx™


ChIP-Seq Metagenomics Sequencing
Whole Genome OncoGxOne
utions Sequencing Sequencing
Proprietary 16S assay with greater sensitivity and specificity
than traditional techniques.

uencing Metagenomics genoTYPER-NEXT™


FuzeSeq Antibody Adventitious Agent Bioinformatics
nels Sequencing Sequencing Contamination Testing Solutions
Effective and efficient option to screen targeted cell lines
through an automated, interactive platform.

Iso-Seq
Identify novel isoforms, complex splicing events, and improved
genome annotations.

ration RNA-Seq Single-Cell RNA-Seq


Small RNA-Seq Exome Sequencing Standalone NGS Servic
cing
Explore the transcriptome of cellular subpopulations in highly
heterogeneous samples.

ration RNA-Seq Small RNA-Seq Exome Sequencing Standalone NGS Servic


cing

NovaSeqTM | HiSeqTM | MiSeqTM Sequel® System Chromium™ Controller

CONTACT GENEWIZ: +1 (908) 222-0711 ext. 1


Ph.D. experts available to discuss your project: [email protected]
genewiz.com
Whole Genome Sequencing Targeted Resequencing
We use the most powerful technologies Our assays offer high sensitivity and
for germline/somatic variant detection, specificity, providing in-depth coverage
de novo genome assembly, whole and high-quality data to help discover
SOLUTIONS

genome resequencing, structural point mutations, INDELs, CNVs, and


variant discovery, and CNV detection. gene rearrangements.

• Illumina® Short-Read Technology • Whole Exome Sequencing


Title 10x
Small RNA-Seq Exome Sequencing Standalone NGS Services Cancer Panels Targeted Resequencing
matics • PacBio Long-Read
Amplicon Technology
ChIP-Seq Whole Genome • 16S MetaVxTM Metagenomics Sequencing
OncoGxOne
ons
& Cancer Panels
• 10xSequencing
Genomics® DNA Phasing Sequencing
• genoTYPER-NEXTTM for Genome Editing Verification
• Single Cell V(D)J Sequencing
• Cancer & Custom Gene Panels:

Genome Assembly SNP/Variant Genotyping


APPLICATIONS

Structural Variant Discovery Metagenomics


Genome/Haplotype Phasing Clone Verification
Genotyping Antibody Repertoire Analysis
Metagenomics

Whole Genome Sequencing 16S MetaVx™ Metagenomics Sequencing


on the PacBio Sequel
Detect more bacterial and archaeal genera than traditional
16S assays.
Coupled with GENEWIZ’s optimized multiplexing strategy, receive
7x more data than the RSII at lower cost, with lower required input
Download the Case Study
amounts and faster TAT. & Sample Report
LEARN MORE

  genewiz.com/metavx
Download the Case Study
& Tech Note
 genewiz.com/wgs
genoTYPER-NEXTTM
Automated, interactive, and intuitive platform to effectively and
efficiently screen targeted cell lines.

Download the Case Study


& Webinar
  genewiz.com/genotyper

CONTACT GENEWIZ: +1 (908) 222-0711 ext. 1


Ph.D. experts available to discuss your project: [email protected]
genewiz.com
RNA Sequencing Amplicon Sequencing
GENEWIZ offers multiple options for
Accurately analyze low expression genes
and transcripts often not detected ultra-deep sequencing of PCR products
by other methods, discover novel using the latest technologies to provide
SOLUTIONS

genes and isoforms, and assemble custom, in-depth solutions for amplicons
transcriptomes not previously studied. ranging from 100 to 10,000 bp.

• Standard & Strand-Specific • Expedited Sequencing Options


• mRNA & Long Non-Coding RNA • Customizable Amplicon Sequencing
enomics FuzeSeq Antibody Next-Generation
Adventitious Agent RNA-Seq
Bioinformatics Small RNA-Seq
Amplicon
• Small RNA (miRNA) Sequencing • Contiguous Long-Read Sequencing (up to 10 kb)
encing Sequencing Contamination Testing Solutions Sequencing
• Ultra-Low Input
• Single-Cell Level
• Isoform Sequencing (Iso-Seq)

Differential Gene Expression Genotyping


APPLICATIONS

Transcriptome Assembly Antibody Repertoire Analysis


Genome Annotation Somatic Variant Discovery
Alternative Splicing Analysis Genome Editing Verification
Novel Variant/Isoform Discovery Variant Phasing
Metagenomics

Ultra-Low Input RNA-Seq Evolution of Amplicon Sequencing


Bulk expression analysis of samples containing as low as 10 pg of Explore popular applications of NGS-based
RNA or just a few cells. amplicon sequencing.

Download the Tech Note  Download the Webinar

  genewiz.com/rna-seq  genewiz.com/amplicon-ez
LEARN MORE

Single-Cell RNA-Seq Iso-Seq


Explore the transcriptome of cellular subpopulations in highly Identify novel isoforms, complex splicing events, and improved
heterogeneous samples. genome annotations through long-read technology.

 Download the Case Study & Webinar Download the Tech Note

 genewiz.com/single-cell   genewiz.com/iso-seq

CONTACT GENEWIZ: +1 (908) 222-0711 ext. 1


Ph.D. experts available to discuss your project: [email protected]
genewiz.com
ABOUT GENEWIZ
For nearly 20 years, GENEWIZ has been a leader in R&D genomics

services, providing superior data quality with unparalleled technical

support to enable researchers around the world to advance their

scientific discoveries faster than ever before.

Our customers at top-tier pharmaceutical, biotechnology, and

academic institutions, as well as cutting-edge start-ups, rely on our

proprietary technologies for consistent, reliable, high-quality data,

even on the most difficult projects. A full-service provider, we provide

Sanger DNA sequencing, next generation sequencing, gene synthesis,

molecular biology, bioinformatics, and GLP regulatory services via our

network of laboratories across the globe.

GENEWIZ LOCATIONS

Takeley, United Kingdom

Germany
Seattle, WA
Boston, MA
San Francisco, CA
South Plainfield, NJ Beijing, China
Los Angeles, CA Washington, D.C. Metro Tianjin, China
San Diego, CA Research Triangle Park, NC Suzhou, China
Guangzhou, China Tokyo, Japan

CONTACT GENEWIZ: +1 (908) 222-0711 ext. 1


Ph.D. experts available to discuss your project: [email protected]
genewiz.com

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