resequencing storage SNP ncrna metagenomics private trio de novo exome ncrna RNA DNA bioinformatics RNA-seq comparative genomics

Similar documents
DNA. bioinformatics. epigenetics methylation structural variation. custom. assembly. gene. tumor-normal. mendelian. BS-seq. prediction.

About Strand NGS. Strand Genomics, Inc All rights reserved.

Welcome to the NGS webinar series

Bioinformatics Advice on Experimental Design

Next Generation Sequencing. Target Enrichment

Cancer Genetics Solutions

Ion S5 and Ion S5 XL Systems

Whole Transcriptome Analysis of Illumina RNA- Seq Data. Ryan Peters Field Application Specialist

Gene Regulation Solutions. Microarrays and Next-Generation Sequencing

IMGM Laboratories GmbH. Sales Manager

Target Enrichment Strategies for Next Generation Sequencing

Next-Generation Sequencing. Technologies

Ion S5 and Ion S5 XL Systems

How much sequencing do I need? Emily Crisovan Genomics Core

QIAGEN s NGS Solutions for Biomarkers NGS & Bioinformatics team QIAGEN (Suzhou) Translational Medicine Co.,Ltd

A Genomics (R)evolution: Harnessing the Power of Single Cells

RNA-Sequencing analysis

Impact of gdna Integrity on the Outcome of DNA Methylation Studies

MULTIPLEXING SIMULTANEOUSLY DETECT MULTIPLE TARGETS IN SINGLE ASSAYS. WhiteSci Whitehead Scientific (Pty) Ltd. Products. Expertise. Support.

Introduction to the UCSC genome browser

Introductie en Toepassingen van Next-Generation Sequencing in de Klinische Virologie. Sander van Boheemen Medical Microbiology

High-throughput scale. Desktop simplicity.

CMPS 3110 : Bioinformatics. High-Throughput Sequencing and Applications

Next-Generation Sequencing Services à la carte

Exploring new frontiers with next-generation sequencing

Research school methods seminar Genomics and Transcriptomics

Digital DNA/RNA sequencing enables highly accurate and sensitive biomarker detection and quantification

Microarray Gene Expression Analysis at CNIO

Sanger vs Next-Gen Sequencing

Analysing genomes and transcriptomes using Illumina sequencing

Functional Genomics Overview RORY STARK PRINCIPAL BIOINFORMATICS ANALYST CRUK CAMBRIDGE INSTITUTE 18 SEPTEMBER 2017

High Cross-Platform Genotyping Concordance of Axiom High-Density Microarrays and Eureka Low-Density Targeted NGS Assays

ACCEL-NGS 2S DNA LIBRARY KITS

Introduction to Bioinformatics and Gene Expression Technologies

Microbial Metabolism Systems Microbiology

WELCOME. Norma J. Nowak, PhD Executive Director, NY State Center of Excellence in Bioinformatics and Life Sciences (CBLS)

SMARTer Ultra Low RNA Kit for Illumina Sequencing Two powerful technologies combine to enable sequencing with ultra-low levels of RNA

Introduction to Bioinformatics

Standard Products Nucleic Acid Sample Submission Guideline

Long and short/small RNA-seq data analysis

PrimePCR Assay Validation Report

Mapping strategies for sequence reads

Gene Expression Technology

Applications and Uses. (adapted from Roche RealTime PCR Application Manual)

Microarrays: since we use probes we obviously must know the sequences we are looking at!

AGILENT S BIOINFORMATICS ANALYSIS SOFTWARE

Agilent Genomics Software Future Directions

The Agilent Technologies SureSelect Platform for Target Enrichment

Next Gen Sequencing. Expansion of sequencing technology. Contents

Gene Expression Analysis Superior Solutions for any Project

INTRODUCTION TO REVERSE TRANSCRIPTION PCR (RT-PCR) ABCF 2016 BecA-ILRI Hub, Nairobi 21 st September 2016 Roger Pelle Principal Scientist

Genomics and Transcriptomics of Spirodela polyrhiza

Introduction to Microarray Analysis

Index. E Electrophoretic Mobility Shift Assay (EMSA), 262 ENCODE project, 223, 224 European Nucleotide Archive (ENA), 34

Single Cell Genomics

Data Analysis with CASAVA v1.8 and the MiSeq Reporter

NGS: Digital RNAseq & Library Prep Seminar. Next-Generation Sequencing Lunch & Learn

Targeted Sequencing Using Droplet-Based Microfluidics. Keith Brown Director, Sales

Non-Organic-Based Isolation of Mammalian microrna using Norgen s microrna Purification Kit

Product selection guide Ion GeneStudio S5 Series

INTRODUCCIÓ A LES TECNOLOGIES DE 'NEXT GENERATION SEQUENCING'

Combined High-Resolution Single Cell Genome And Transcriptome Analysis For Clinical Samples

PrimePCR Assay Validation Report

Product selection guide Ion S5 and Ion S5 XL Systems

Workshop on Genomics. Český Krumlov Monday, January 7, 13

Introduction to BioMEMS & Medical Microdevices DNA Microarrays and Lab-on-a-Chip Methods

Pyrosequencing. Alix Groom

Green Center Computational Core ChIP- Seq Pipeline, Just a Click Away

PrimePCR Assay Validation Report

Oncomine cfdna Assays Part III: Variant Analysis

Considerations for Illumina library preparation. Henriette O Geen June 20, 2014 UCD Genome Center

Corporate Medical Policy

Fusion Gene Analysis. ncounter Elements. Molecules That Count WHITE PAPER. v1.0 OCTOBER 2014 NanoString Technologies, Inc.

Gene Expression on the Fluidigm BioMark HD

Please purchase PDFcamp Printer on to remove this watermark. DNA microarray

Gene Expression Profiling and Validation Using Agilent SurePrint G3 Gene Expression Arrays

Lecture #1. Introduction to microarray technology

Next Generation Sequencing: An Overview

MICROARRAYS+SEQUENCING

ChIP-Seq Data Analysis. J Fass UCD Genome Center Bioinformatics Core Wednesday 15 June 2015

Multi-omics in biology: integration of omics techniques

LATE-PCR. Linear-After-The-Exponential

3.1.4 DNA Microarray Technology

RNA-Seq Software, Tools, and Workflows

Targeted Sequencing in the NBS Laboratory

E2ES to Accelerate Next-Generation Genome Analysis in Clinical Research

Introduction to Next Generation Sequencing (NGS)

SNP GENOTYPING WITH iplex REAGENTS AND THE MASSARRAY SYSTEM

measuring gene expression December 5, 2017

RNA SEQUINS LABORATORY PROTOCOL

Student Learning Outcomes (SLOS)

Genome Sequencing Technologies. Jutta Marzillier, Ph.D. Lehigh University Department of Biological Sciences Iacocca Hall

PrimePCR Assay Validation Report

Next Generation Sequencing Technologies. Some slides are modified from Robi Mitra s lecture notes

Machine Learning Methods for RNA-seq-based Transcriptome Reconstruction

Fundamentals of Next-Generation Sequencing: Technologies and Applications

Péter Antal Ádám Arany Bence Bolgár András Gézsi Gergely Hajós Gábor Hullám Péter Marx András Millinghoffer László Poppe Péter Sárközy BIOINFORMATICS

Complete Sample to Analysis Solutions for DNA Methylation Discovery using Next Generation Sequencing

Examples of founding and evolving leading LifeScience companies. November 2016

Transcription:

RNA Sequencing T TM

variation genetics validation SNP ncrna metagenomics private trio de novo exome mendelian ChIP-seq RNA DNA bioinformatics custom target high-throughput resequencing storage ncrna comparative genomics structural variation indel epigenetics amplicon personalized tumor-normal diagnostics NGS genomics prediction RIP-seq RNA-seq assembly gene expression

IGATech is the leading Italian provider of genomic research services using Illumina Next Generation Sequencing (NGS) technology. We are the largest lab in Italy offering these services on a wide range of organisms: we have experience with humans, other animals, plants and microorganisms. The company has direct access to the scientific NGS Next Generation Services T TM and technological resources of its founder, the Institute of Applied Genomics (IGA), which has gained an outstanding reputation in genomic research through participation in genome sequencing projects both at a national and international level. Among the genomic research services provided, the company also offers a wide variety of bioinformatic services such as conventional and custom analyses and customer-oriented software development.

IGATECH Transcriptomics ILLUMINA SEQUENCING TECHNOLOGY The Illumina massively parallel sequencing technology makes multiple gigabases of data from several million templates economically available, enabling new approaches to genomic characterization. The Illumina technology allows tipically genome center-like studies to be accomplished at the individual laboratory level. A single technology workflow is capable of supporting genome-wide analyses as different as DNA sequencing (de novo and resequencing), gene expression, transcriptome characterization and expression control including small RNA discovery, protein-dna interactions and CpG methlyation status. We are a certified service provider (CSPro) of Illumina genomic sequencing. Highly customizable Targeted RNA-Seq expression assays generate data equivalent to individual RT-PCR assays and offer an accurate and powerful method for validating gene expression arrays and RNA-Seq studies. De novo assembly of RNA-Seq data allows for transcriptome studies for non-model organisms lacking well-defined genomes or for cancer samples, permitting downstream RNA-Seq analyses. RIP-Seq, i.e. sequencing of RNA-binding protein immunoprecipitation, maps RNA-protein associations in vivo by discovering genome-wide RNA molecules of any type that physically interact with a regulatory protein or protein complex. RNA SEQUENCING Qualitative and quantitative transcriptome characterization RNA-Seq is a powerful method for discovering, profiling, and quantifying RNA transcripts across the entire transcriptome. Constant technological improvements allow for robust analysis on a wide range of samples, including low-quality and FFPE. The amount of valuable information that can be obtained from RNA-Seq data is truly enormous. In addition to gene expression analysis, deep sequencing of RNA samples enables the detection of alternative splicing events, rare or novel transcripts, and gene fusions. It also allows discovery of SNPs, identification of non-coding RNAs and their targets, and measurement of allele-specific expression.

IGATECH Services list LIBRARY PREPARATION AND SEQUENCING mrna-seq Strand oriented RNA-seq Small RNA-seq Targeted RNA Expression RIP-Seq Low-quality and FFPE BIOINFORMATICS SERVICES Quality control and alignment to a reference Differential expression analysis Allele-specific expression analysis Cross-species comparison Detection of new exons, splice variants and gene fusions SNP detection Deriving strand information with high precision Non-coding RNA analysis De novo assembly Prediction of new micrornas and lncrnas and their targets RIP-Seq analysis Our team is always available to consult with you on study design to ensure correct sequencing and bioinformatics strategies are used to meet your goals.

T TM IGA TECHNOLOGY SERVICES SRL c/o Parco Scientifico e Tecnologico L. Danieli Via Linussio 51 33100, Udine (Italy) Tel. +39 0432 629911 www.igatechnology.com