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オンラインセミナー & ビデオ
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文献 & 発表
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ニュースリリース
Video Highlights - SOLiD™
System in Action
サムネイルをクリックしてビデオをご覧ください。
News & Product Information
Interactive Tour:
SOLiD™ Data Analysis
and BioScope Software Tour |
Webinar: Profiling Small
RNAs with SOLiD™
System and miR-Intess™
from InterRNA Genomics |
Webinar: SOLiD™
System and Partek®
Genomics Suite™ (Registration Required) |
Webinar: mRNA-Seq Analysis
of a Single Cell (Registration
Required) |
Webinar: Advances in Cancer
Genomics (Registration Required) |
Webinar: Fundamentals of
2 Base Encoding and Color Space |
Video: SOLiD™ System Sequencing
on San Francisco FOX Television
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Video: SOLiD™
System Used to Sequence a Human
Genome for $60,000 |
Video: Introduction to
the SOLiD™ System |
Webinar: Whole Transcriptome
Analysis (Registration Required) |
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Researcher Spotlight
Alain Nicolas, CNRS Research
Scientist, Institut Curie, Paris
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William G. Farmerie, Associate
Director Interdisciplinary Center
for Biotechnology Research, University
of Florida |
Greg Foltz & Anup Madan,
co-directors of the Center for
Advanced Brain Tumor Treatment
at the Seattle Neuroscience Institute |
Jesse Gray, Postdoctoral
Fellow, Children's Hospital Boston
and Harvard Medical School |
Yijun Ruan, Senior Group
Leader and Associate Director,
Genomic Technologies at the Genome
Institute of Singapore |
Donna Muzny, Director of
Operations, Human Genome Sequencing
Center, Baylor College of Medicine |
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アプリケーション毎のSOLiDの論文、アカデミックポスターがご覧になれます
全トランスクリプトーム解析
アプリケーションノート
ポスター
- Genome-wide
discovery of copy number
variations in cancer
patients using SOLiD
sequencing
Xu, X., et al.
(2009)
- Multiplex
Sequencing on the SOLiD™
Platform with 10, 16,
or 96 Barcodes
Zhang, L., et al.
(2009)
- Whole
Transcriptome Analysis
of Total Human RNAs
by Massively Parallel
Sequencing on the SOLiD™
System
Nutter, B., et al.
(2009)
- SOLiD™
Sequencing Unravels
Transcriptome.
Innovations- Fall 2007
- Single
Cell Transcriptome Analysis
on the SOLiD™
System.
Lao, K., et al.
文献
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スモールＲＮＡ解析
アプリケーションノート
ポスター
文献
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クロマチン免疫沈降シーケンシング（ChIP-Seq)
アプリケーションノート
- SOLiD™
システムによるChIP-Seq (E)
(J)
文献
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遺伝子発現プロファイリング
アプリケーションノート
ポスター
SOLID
PROOF News
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全ゲノムリシーケンシング
アプリケーションノート
ポスター
- Genome-wide
discovery of copy
number variations
in cancer patients
using SOLiD sequencing
Xu, X., et
al. (2009)
- Increased
Read Length on
the SOLiD™
Sequencing Platform
Dimalanta, E.,
et al.
(2009)
- The
Detectable Genome:
How much of the
human genome is
accessible to
variant discovery
by next-generation
sequencing?
Peckham, H., et
al. (2009)
- Large-Scale
SNP Detection
via Ligation-based
Dibase Sequencing
Across Multiple
HapMap Individuals:
NA18507, NA19240,
and NA12878.
McLaughlin, S.,
et al.
(2009)
- Accurate
genome-wide SNP
detection with
low and medium
coverage with
next-generation
sequencing.
Hyland F.C.L.,
et al.
(2009)
- Dibase
sequencing allows
accurate SNP detection
at moderate and
low coverage with
diBayes algorithm
Hyland F.C.L.,
et al.
(2009)
- Functional
analysis of the
genetic variation
within the genomes
of three HapMap
individuals obtained
by whole-genome,
second-generation
sequencing
De La Vega, F.
M (2009)
- Sequence
and Structural
Variation in a
Human Genome
Peckham, H., et
al. (2009)
- Resolving
Structural Variations
Using SOLiD™
Mate Pair Sequencing
Technology
Fu, Y., et
al. (2009)
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ポスター(続き）
- A
high-resolution
structural variation
map of human germline
genomes by next-generation,
high-throughput
paired end sequencing
with the SOLiD™
System
Peckham, H., et
al. (Cold
Spring Harbor,
Biology of Genomes
2008)
- Whole
Genome Resequencing
with Short Reads:
Accurate Mutation
Discovery with
Mate Pairs and
Quality Values
McLaughlin, S.,
et al.
(ASHG 2007)
- Finding
Indels with Short
Sequencing Reads
and De Novo
Assembly with
SOLiD Reads
Zhang, Z., et
al. (ASHG
2007)
- Genome
Variablility Analysis
of Yoruba in Ibadan,
Nigeria (NA18507)
by SOLiD Mediated
Whole Genome Re-Sequencing
Ranade, S., et
al.
- Next-generation
Sequencing for
Detection of Rare
Variants and Heterozygosity
(ASHG 2007)
文献
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ターゲットリシーケンシング（候補領域のリシーケンシング）
アプリケーションノート
ポスター
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デノボシーケンシング
アプリケーションノート
ポスター
文献
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SOLiD™
システムとは
文献
- “Applied
Biosystems SOLiD™
System: Ligation-Based
Sequencing,” Next Generation
Genome Sequencing: Towards
Personalized Medicine,
Pandey V, Nutter RC,
Prediger E (2008), Wiley,
pages 29-41
- “New
Frontiers in Plant Functional
Genomics Using Next
Generation Sequencing
Technologies,” The
Handbook of Plant Functional
Genomics, Concepts and
Protocols. R. Nutter,
G. Kahl et. al. (2008)
Wiley, pages 431-444
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SOLiD™
システムの特徴
アプリケーションノート
- SOLiD™
システムバーコディング (E)
(J)
- 2ベースエンコーディングとカラースペースのメリット
(E)
(J)
ポスター
白書
文献
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