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16S, 1x Illumina HiSeq 4000, 1x Illumina MiSeq, 1x Ion Proton, 1x NextSeq 500, 2x Illumina HiSeq 2500, 2x Illumina MiSeq, 2x Illumina MiSeq: Whole genome sequencing, 2x NextSeq 500, 3 Illumina HiSeq 2500 (Running v4 chemistry), 3730XL, 3730XL(ABI), 3730xl, 3C-seq, 454, 454 FLX Plus, 454 FLX Titanium Plus, 454 and Bioinformatics, 4x Ion Proton, 5x Illumina Hiseq2000/2500, 7x Ion PGM/Protom: Whole genome sequencing, 7x Ion PGM/Proton, : Whole genome sequencing, AB 3730XL Sanger Sequencing, ABI 3730, ABI 3730 xl, Affymetrix GeneChip Systems, Affymetrix microarray inc. Gene Titan high throughput arrays, Agilent SureSelect, Agilent SureSelect Target Enrichment, Agilent SureSelect array design, Ampliseq Panel Design, Animal BSL3, Assay Development & Validation, BAC Libraries, BSL3, Basic & Advanced NGS-Bioinformatics, Basic and Advanced Bioinformatics, Basic and Advanced NGS-Bioinformatics, Bio-Mark, Bioinformatics, Bioinformatics (powered by both CLCbio and NextGENe), Bioinformatics Apps, Bioinformatics Service, Bioinformatics Services, Biostatistics, CLC bio, Cancer gene panels, Candidate gene analysis, Cell Line Authentication, ChIP sequencing, ChIP-Sequencing, ChIP-seq, Clone Free Mate Pair Libraries, Cloud Computing, Complete Human Sequencing, Computational Biology, Cross-Omics Integration, Custom Ampliseq Panels, Custom Projects, Custom Projects and Personalized Solutions, Custom Projects and Personalized Solutions., Custom bait design, DNA and RNA including from blood, DNA extraction, Deep functional analysis of RNA-seq, Dr. Oligo 96/192, Exome Seq (Illumina TruSeq preferred), Extraction specialists, FOSMID Libraries, Fluidgm EP1, Fluidigm Access Array Platform, Fragment Analysis, Functional Genomics, GALAXY, GLP, GS-FLX, GSFLX, Gene Titan high throughput arrays, Genetic Data Storage, Genome Assembly, Genome Sequencing, Genome assembly, Genome sequencing, Genome sequencing; Transcriptome sequencing; Personal Genome Sequencing, Genome sequencing; Transcriptome sequencing;Genotyping, Genome-wide assocation, Genotyping, HPC, Helicos, Helicos Sequencing (DNA and RNA), HiSeq 2000/2500, HiSeq X Ten, HiSeq2500, High performance Computing Cluster, High-performance computing optimization, Human Exome Analysis, Human Whole Genome Clinical Analysis, Human exome analysis, IIllumina MiSeq, ITS, Illumina, Illumina / PacBio / Ion Torrent PGM, Illumina BeadArray, Illumina GA2x, Illumina GAII, Illumina GAIIx, Illumina HiScan SQ, Illumina HiSeq, Illumina HiSeq 2000, Illumina HiSeq 2000/2500, Illumina HiSeq 2500, Illumina HiSeq and MiSeq, Illumina HiSeq2000, Illumina Hiseq, Illumina MiSeq, Illumina Miseq, Illumina NextSeq 500, Illumina microarray, Informatics, Inherited Disease Panels, Inherited disease panels, Internet Services, Ion, Ion PGM, Ion Proton, Ion Torrent, Ion Torrent PGM, Iscan, Library Construction, Library QC/QA, Life Ion Torrent PGM, LifeTech SOLiD 5500 XL, LifeTech SOLiD, LifeTech SOLiD (via Partner), LifeTech SOLiD 4 and 5500 XL, LifeTech SOLiD 5500 XL, Lightcycler 480, MiSeq, Microarrays, Microbial Sequencing, Microbiome Sequencing, Microsatellite Capture, Mid-plex linkage peak, Molecular diagnostics, NGS Analysis, NGS Bioinformatics, NGS Data Analysis, Next-generation sequencing, NextSeq 500, Nextera, Nexus DNA Chip, Nimblegen Microarray, Online Bioinformatics Platform, PCR, PacBio, PacBio RS, PacBio RS / 454, PacBio RS II, Personal Genome Sequencing, Proton, RNA Sequencing, RNA sequencing, RNA-Seq, RNAseqDX, ROCHE 454 FLX+ and Junior, Real-Time PCR, Roche 454 GS FLX Titanium Plus, Roche 454, Roche 454 GS FLX, Roche 454 GS FLX Titanium, Roche 454 GS Junior, Roche 454 and Bioinformatics, SNP detection, SOLiD, SOLiD 4, SOLiD(ABI), Sanger 3730XL, Sanger Sequencing, Sequencing, Sequencing Data Analysis, Sequenom, Single-plex candidate gene analysis, Small RNA analysis, State-of-the-Art Sofware and Database and pipeline Development, Targeted candidate gene expression, Targeted resequencing, Tertiary Analysis (Clinical Interpretation) and Reporting of Genetic Data, Transcriptome analysis, Transcriptome sequencing, Transcriptome sequencing; Personal Genome Sequencing, Transcriptome sequencing; Whole exome sequencing, Transgenic Genotyping, TruSeq Custom Amplicon, WGA, Whole Genome Analysis, Whole exome sequencing, Whole genome expression analysis, Whole genome methylation analysis, Whole genome sequencing, amplicon sequencing, bioinformatics, biostatistics, capable of standard or rapid runs. RNA-Seq, cells and FFPE. Fluidigm and ABI 7900 qPCR instruments. GWAS, custom amplicon, data analytics, data mining, de novo sequencing, experiment design, experimental design, genome, heli, library preparation, llumina HiSeq 2000/2500, metagenomics, microbiome, mirna-seq, qPCR, statistical analysis, targeted sequencing, tunable Genotyping by Sequencing, whole genome library prep:
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