Twist Bioscience (Silver Sponsor!)
(Exhibition + Technology Presentation)

(Exhibition + Technology Presentation)

一分子リアルタイムDNAシークエンサー PacBio Sequelシステムや、 Dovetail Genomics社のゲノムアセンブリ、ヒトゲノム構造解析サービスなどを出展いたします。

(Exhibition + Technology Presentation)

■Technology Presentation
ゲノム構造多型(Structural Variation)は、癌、免疫疾患、神経疾患など多くの病気に関わり、SV解析はこれら疾患解明への貢献が期待されています。Human Chromosome Explorer(HCE)は、正確かつ高速にヒトSV解析を実現するクラウドサービスです。

Human Chromosome Explorer (HCE)

① クラウドベースのヒト構造多型 (hSV) 検出に特化したソフトウェア
② データをクラウド上で自動アセンブル、マッピングし、hSVを検出
③ 検出されたhSVを図表で一覧表示


 (Exhibition + Technology Presentation)

Gain a Multidimensional View of Complex Biology. Whether you want to overcome the limitations of current short-read technology, dissect cell-type differences, or investigate the adaptive immune system, 10x Genomics has the solutions to meet your needs. Learn how to enhance your biological discoveries with our genomics, high-throughput single cell transcriptomics and spatial transcriptomics products and explore our newest technologies.

Illumina, Inc.
 (Exhibition+Technology Presentation)

Oxford Nanopore Technologies. (Exhibition+Technology Presentation)

Oxford Nanopore Technologies has developed the world's first nanopore DNA and RNA sequencing devices. The MinION is a portable, real-time, long-read, low-cost device designed to bring easy biological analyses to anyone, whether in scientific research, education or real world applications such as disease/pathogen surveillance, environmental monitoring, food chain surveillance, self-quantification or microgravity biology. The GridION and PromethION devices serve users with larger projects or more samples. Oxford Nanopore Technologies products are currently for Research Use Only.

Agilent Technologies, Inc.

Cancer genomic biomarkers span SNVs, indels, CNVs and genomic translocations. Currently, multiple technologies are necessary to profile variants, such as IHC, FISH, Sanger sequencing and qPCR. This multi-modal and often sequential approach is expensive and time consuming. Agilent’s new SureSelect Cancer All-In-One (AIO) solution uses Next-Generation Sequencing to provide a streamlined and cost-effective approach for cancer genetic profiling. The SureSelect Cancer AIO Solution leverages specialized probe design and advanced CNV and translocation algorithms. It can be used for catalogue NGS assays (a lung cancer assay and a solid tumour assay), as well as for easily created custom panels.

Genomedia Inc.

GeneBay, Inc.

(1) オックスフォードナノポア シーケンス受託
(2) NGSを用いたゲノムワイド迅速ジェノタイピング法
(3) NGSデータ解析クラウド
(4) ストレージ型NGS解析システムなど

BioStream Co., Ltd

1. ベクトンディッキンソン社製 BD Rhapsody System
マイクロウェルカートリッジを用いて最大20,000細胞を単離しTargeted RNAseq解析及び、WTA解析用のライブラリ調製が可能なシステムです。


2. ArcherDx社製 体細胞変異(融合遺伝子、SNVs、CNVs、Indels)検出用ライブラリ調製試薬


3. incellDx社製 incellPREPシステム



CAGE 5’-RNA sequence service/library preperation kit:
Promoter / Enhancer Annotation in the NGS era!


Bring big data analysis to genome.









Program New!!
  Short Talk
  Meet the Expert
Organizing Committee
Silver Sponsor

TWIST Bioscience

The 13th International Workshop on Advanced Genomics (13AGW)

2-1-1, Suido, Bunkyo-ku, Tokyo 112-0005, Japan
Phone: +81-3-3814-7112 FAX: +81-3-3814-6904
E-mail: 13agw@keiso-comm.com