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Taueret Laboratories, L.L.C.

Salt Lake City, Utah, US
New

Taueret Laboratories focuses on clinical and discovery work for human infertility and genetic conditions affecting women and children. Testing is performed using state-of-the-art instrumentation at our CAP and CLIA accredited facility. The lab is active in new test and technology development and collaborates with numerous federal, state, and local agencies, universities, commercial laboratories, and private clients.

Taueret Laboratories, L.L.C. has not listed any services.

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Whole Exome Sequencing (WES)
Price on request

Whole Exome Sequencing (WES) is designed to sequence all the protein-coding regions in a genome, collectively referred to as an exome. The exome represents less than 2% of the genome and is comprised of approximately 180,000 exons. Since 85% of all disease-causing sequence variants are located in protein-coding regions of the... Show more »

Whole Exome Sequencing (WES) is designed to sequence all the protein-coding regions in a genome, collectively referred to as an exome. The exome represents less than 2% of the genome and is comprised of approximately 180,000 exons. Since 85% of all disease-causing sequence variants are located in protein-coding regions of the genome, WES is an efficient method for identifying the underlying causes of both common and rare diseases. Taueret Laboratories provides high quality WES services to achieve high exome coverage required for accurate and reliable variant discovery.

WES Service Details:
• Exome libraries are produced using the Ion Ampliseq Exome Library Kit.
• The Ampliseq Kit is designed to target ~33Mb of coding exons. Greater than 97% of coding regions as described by consensus coding sequences (cCDS) annotation are amplified in 12 primer pools, 294,000 primer pairs, for highly specific enrichment of exons within the human genome.
• The whole exome is then sequenced using the Ion Proton or Ion S5 sequencing platform with 200 bp amplicon read technology using a P1V3 chip.
• Following data collection, the exome DNA sequences generated for each sample are aligned and compared to human genome build UCSC hg19 reference sequence using the Ion Torrent Suite software v4.2.
• Deliverables include FASTQ, VCF, BAM, and BAI files as desired. Additional bioinformatic analyses is available upon request; please contact us for pricing.
• Mean depth coverage ranges from 30x up to > 100x depending on customers requirements.
• Taueret’s WES services are provided as Research Use Only (RUO), but all work is conducted in a CAP/CLIA environment.

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Genomics
Whole Exome Sequencing
human
Ion Torrent Proton
Ion Torrent Chef
Ion Torrent S5
AmpliSeq
Exome Sequencing Services
Ion Torrent Sequencing
Ion Torrent Next Generation Sequencing
Price on request

The Ion Torrent platform allows for sequence analysis for targeted gene panels in situations where whole genome or whole exome analysis is not required. This platform allows for the creation of customized panels that can be tailored to specific DNA segments, genes or alleles to meet your sequencing requirements.
Sample... Show more »

The Ion Torrent platform allows for sequence analysis for targeted gene panels in situations where whole genome or whole exome analysis is not required. This platform allows for the creation of customized panels that can be tailored to specific DNA segments, genes or alleles to meet your sequencing requirements.
Sample Processing:
• If not specifically provided by the customer Taueret will perform bioinformatics analysis to determine the total number of amplicons required to ensure complete coverage of the SNPs, genes or alleles targeted by the customer.
• All amplicons are simultaneous amplified in a single large pool using primer pairs customized to the customers targeted sequences.
• All amplification and library preparation steps are conducted using Biomek robotic liquid handing stations to ensure high throughput efficiencies and quality control.
• Library preparation for sequencing is performed using the Ion AmpliSeq Kit for Chef DL8 library kit. Each sample is labeled with a unique DNA barcode and the Ion Chef System is utilized to automate workflow and chip loading prior to sequencing.
• Sequencing is conducted on the Ion Proton or Ion S5 instrument using the Ion P1 Chip Kit 2x150bp chemistry.
• Data is reported in a secure electronic format in the form of FastQ, VCF or BAM files.
• Data Interpretation & Analysis is available upon request; fees are dependent on the scope of the project.

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Bioinformatics
Ion Torrent Proton
Ion Torrent Chef
Ion Torrent S5
Biomek-FX Laboratory Automation Systems
AmpliSeq
DNA Extraction and Purification
Price on request

Taueret Laboratories offers both manual and automated DNA Extraction services for the following sample types:
• Blood
• Buccal swab
• Saliva
• Tissue
• Cells
• FFPE
• Buffy Coat (WBC)
• Plants
• Fungi
• Body Fluids
• Bacteria

High throughput automated DNA extraction performed using the Chemagic MSM I 96-well... Show more »

Taueret Laboratories offers both manual and automated DNA Extraction services for the following sample types:
• Blood
• Buccal swab
• Saliva
• Tissue
• Cells
• FFPE
• Buffy Coat (WBC)
• Plants
• Fungi
• Body Fluids
• Bacteria

High throughput automated DNA extraction performed using the Chemagic MSM I 96-well Automated DNA Extraction Workstations (Perkin Elmer). Sample preparation is based on M-PVA Magnetic Bead technology.

Our laboratory is well-equipped to determine quantity and quality of extracted DNA:
• NanoDrop ND-1000 Spectrophotometer
• PicoGreen analysis with the BioTek Synergy-2 Fluorometer
• Agarose Gel Electrophoresis using UVP Gel Documentation System
• Bio-Rad Molecular Imager Gel Doc XR System

Sample integrity is maintained during sample preparation and storage by creating labels with the Zebra ZM400 Thermal Printers.

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Nanodrop ND-1000 Spectrophotometer
Buccal swab
FFPE tissue
Fungi
saliva
Plants
human
Chemagic 96-well Automated DNA Extraction Workstation
Bio-Rad Molecular Imager
BioTek Synergy-2 Fluorometer
Next Generation Sequencing (NGS)
Price on request

NGS SEQUENCING LIBRARY PREP
• Genome / Exome
• AmpliSeq 2.0 (custom Primer sets/panels)
• Ion Xpress Fragment (De novo)

NGS SEQUENCING
• Exome (human sample, batch processing: 3, 4 or 5 samples/run)
• Genome (non-human, plant/fungi)
• Genome Prime (3-4 fungi samples)
• Custom/targeted

SEQUENCING PLATFORMS
• Ion... Show more »

NGS SEQUENCING LIBRARY PREP
• Genome / Exome
• AmpliSeq 2.0 (custom Primer sets/panels)
• Ion Xpress Fragment (De novo)

NGS SEQUENCING
• Exome (human sample, batch processing: 3, 4 or 5 samples/run)
• Genome (non-human, plant/fungi)
• Genome Prime (3-4 fungi samples)
• Custom/targeted

SEQUENCING PLATFORMS
• Ion Torrent Proton Next Generation Sequencing Systems
• Ion Torrent Chef Support Systems
• Ion Torrent S5

Data delivery options include raw FastQ, VCF, BAM and BAI files. All data is transferred using secured methods.

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Ion Torrent Proton
Ion Torrent Chef
Ion Torrent S5
Single Nucleotide Polymorphism (SNP) Genotyping
Price on request

Taueret Laboratories offers a broad range of Single Nucleotide Polymorphism (SNP) genotyping services that are customizable to meet your needs (research, clinical, direct-to-consumer) for any large or small-scale project.

SNP Genotyping Service Description:
• SNP discovery, primer design, validation and screening available... Show more »

Taueret Laboratories offers a broad range of Single Nucleotide Polymorphism (SNP) genotyping services that are customizable to meet your needs (research, clinical, direct-to-consumer) for any large or small-scale project.

SNP Genotyping Service Description:
• SNP discovery, primer design, validation and screening available if required.
• SNP detection is based on the TaqMan SNP Genotyping Assays from Applied Biosystems.
• SNP sequence detection also available with the 7900HT Fast Real-Time PCR System from Applied Biosystems in either 96 or 384-well format.
• Single tube and/or multiplex SNP genotyping available
• OpenArray Real-Time PCR with QuantStudio 12k Flex provides flexible SNP genotyping capabilities for optimization of the number of samples to be tested vs the number of SNPs required. This system utilizes the robust TaqMan chemistry platform and can be customized to match your requirements.
• Biomek-FX liquid handling robotic workstations available to ensure accuracy and efficiency for high-throughput projects.
• All data is reported in user friendly formats with flexible reporting options including fluorescent scans and/or genotypes in spreadsheet format.

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Human
Applied Biosystems 7900HT Fast Real-Time PCR System
TaqMan
multiplex
QuantStudio 12K Flex
Primer Design
OpenArray
Genotyping Services
Price on request

Taueret Laboratories offers the following genotyping services:

Sequence variation detection:
• 7900HT Fast Real-Time PCR System from Applied Biosystems in either 96 or 384-well format based on TaqMan chemistry.
• OpenArray Real-Time PCR with QuantStudio 12k Flex
• Ion Torrent targeted Next Generation Sequencing... Show more »

Taueret Laboratories offers the following genotyping services:

Sequence variation detection:
• 7900HT Fast Real-Time PCR System from Applied Biosystems in either 96 or 384-well format based on TaqMan chemistry.
• OpenArray Real-Time PCR with QuantStudio 12k Flex
• Ion Torrent targeted Next Generation Sequencing (NGS)

Fragment analysis detection:
• ThermoFisher Scientific 3730xl & 3130xl DNA Analyzers

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Applied Biosystems 3730xl DNA Sequencer
Applied Biosystems 7900HT Fast Real-Time PCR System
Next Generation Sequencing
QuantStudio 12K Flex
ABI 3130XL
Ion Torrent
OpenArray
Bioinformatics Data Analysis
Price on request

Taueret Laboratories experienced Bioinformatics team utilizes advanced methodologies to produce accurate, high quality and reproducible results. We provide streamlined bioinformatics solutions including experimental design, expert consultation, technical and scientific support. Our Bioinformatics solutions are available as a... Show more »

Taueret Laboratories experienced Bioinformatics team utilizes advanced methodologies to produce accurate, high quality and reproducible results. We provide streamlined bioinformatics solutions including experimental design, expert consultation, technical and scientific support. Our Bioinformatics solutions are available as a standalone service or as a component to our Next Generation Sequencing (NGS) services. Reports are delivered in a secure format and deliverables include Quality Control Summary Report, Data Analysis Report and raw sequencing and alignment data.

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Clinical Laboratory Services
Price on request

Taueret Laboratories is CLIA/CAP certified to run the following diagnostic testing services:
• Chromosome Microarray (CMA)
• Fragile X
• Pharmacogenetics (PGx)
• Factor II (Prothrombin)
• Factor V Leiden
• Apolipoprotein E (APOE)

Taueret Laboratories is CLIA/CAP certified to run the following diagnostic testing services:
• Chromosome Microarray (CMA)
• Fragile X
• Pharmacogenetics (PGx)
• Factor II (Prothrombin)
• Factor V Leiden
• Apolipoprotein E (APOE)

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Fragile X
Factor II (Prothrombin)
Factor V Leiden
Apolipoprotein E (APOE)
Pharmacogenetics
Clinical Molecular Diagnostics
Price on request

Clinical Molecular Diagnostics Services

Clinical Molecular Diagnostics Services

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Chromosomal Microarrays
Price on request

Chromosomal microarray analysis is a method of measuring gains and losses of DNA throughout the human genome. It is a high-resolution whole-genome screening that can identify major chromosomal aneuploidy as well as the location and type of specific genetic changes that are too small to be detected by conventional karyotyping.... Show more »

Chromosomal microarray analysis is a method of measuring gains and losses of DNA throughout the human genome. It is a high-resolution whole-genome screening that can identify major chromosomal aneuploidy as well as the location and type of specific genetic changes that are too small to be detected by conventional karyotyping.

The most common reasons for performing cytogenetic studies for prenatal diagnosis include advanced maternal age, abnormal prenatal screen, a previous child with a chromosome abnormality, abnormal fetal ultrasound, or a family history of a chromosome abnormality. Chromosomal microarray (CMA) is a high-resolution method for detecting copy number changes (gains or losses) across the entire genome in a single assay and is sometimes called a molecular karyotype. The American College of Obstetricians and Gynecologists and the Society for Maternal-Fetal Medicine recommend the chromosomal microarray as a replacement for the fetal karyotype in patients with a pregnancy demonstrating 1 or more major structural abnormalities on ultrasound when undergoing invasive prenatal diagnosis.

This CMA test utilizes >1.9 million copy number probes and approximately 750,000 single nucleotide polymorphism (SNP) probes for the detection of copy number changes and regions with absence of heterozygosity (AOH).

Taueret Laboratories is well-equipped to run chromosome microarray and utilizes the Affymetrix™ GeneChip™ Scanner 3000 systems, including hybridization ovens, automated fluidics stations and high-resolution scanners.

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Affymetrix GeneChip System 3000
Chromosome Abnormality
Chromosome Microarray
Copy Number Variant
Gene Expression Analysis
Price on request
Request a quote for more information about this service.
TaqMan Assays
TaqMan Gene Expression Assays
Price on request

Taueret Laboratories specializes in TaqMan testing services including real-time quantitative polymerase chain reaction (qPCR) and SNP genotyping. We utilize the Applied BioSystems 7900 HT platform which allows for either 96- and 384-well formats to accommodate high-throughput projects. Taueret also utilizes the Applied BioSystems... Show more »

Taueret Laboratories specializes in TaqMan testing services including real-time quantitative polymerase chain reaction (qPCR) and SNP genotyping. We utilize the Applied BioSystems 7900 HT platform which allows for either 96- and 384-well formats to accommodate high-throughput projects. Taueret also utilizes the Applied BioSystems OpenArray Genotyping Instruments (QuantStudio 12K Flex Real Time PCR System) including the AccuFill™ Sample Loading System.

Users may also choose to submit their own genes and/or primer pairs or work with Taueret Laboratories for assay design services; please contact us for assay design information and pricing.

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Applied Biosystems 7900HT Fast Real-Time PCR System
QuantStudio 12K Flex
Real time qPCR
SNP Genotyping
PCR
Price on request

CNV
Library Quantitation
Assays (16, 32, 64, 128, 256 array format)

CNV
Library Quantitation
Assays (16, 32, 64, 128, 256 array format)

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Capillary Electrophoresis
Price on request

Taueret Laboratories offers fragment analysis services using either our Applied BioSystems 3730 XL for large sample projects or the ABI 3130 XL DNA Analyzer for smaller projects.

Fragment Analysis Applications Include:
• Microsatellite Analysis
o Parentage verification and identity/relationship testing
• VNTR... Show more »

Taueret Laboratories offers fragment analysis services using either our Applied BioSystems 3730 XL for large sample projects or the ABI 3130 XL DNA Analyzer for smaller projects.

Fragment Analysis Applications Include:
• Microsatellite Analysis
o Parentage verification and identity/relationship testing
• VNTR Genotyping
• Mutation Detection
• Fragile X (CGG repeats)
• SMA Carrier Testing

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ABI 3730XL
ABI 3130XL
Fragile X
Microsatellite Analysis
Mutation Detection
DNA Extraction
Price on request

Taueret Laboratories offers both manual and automated DNA Extraction services for the following sample types:
• Blood
• Buccal swab
• Saliva
• Tissue
• Cells
• FFPE
• Buffy Coat (WBC)
• Plants
• Fungi
• Body Fluids
• Bacteria

High throughput automated DNA extraction performed using the Chemagic MSM I 96-well... Show more »

Taueret Laboratories offers both manual and automated DNA Extraction services for the following sample types:
• Blood
• Buccal swab
• Saliva
• Tissue
• Cells
• FFPE
• Buffy Coat (WBC)
• Plants
• Fungi
• Body Fluids
• Bacteria

High throughput automated DNA extraction performed using the Chemagic MSM I 96-well Automated DNA Extraction Workstations (Perkin Elmer). Sample preparation is based on M-PVA Magnetic Bead technology.

Our laboratory is well-equipped to determine quantity and quality of extracted DNA:
• NanoDrop ND-1000 Spectrophotometer
• PicoGreen analysis with the BioTek Synergy-2 Fluorometer
• Agarose Gel Electrophoresis using UVP Gel Documentation System
• Bio-Rad Molecular Imager Gel Doc XR System

Sample integrity is maintained during sample preparation and storage by creating labels with the Zebra ZM400 Thermal Printers.

« Show less
Nanodrop ND-1000 Spectrophotometer
Quant-It PicoGreen
Buccal swab
FFPE tissue
Fungi
saliva
Blood
Plants
human
Chemagic 96-well Automated DNA Extraction Workstation
Bio-Rad Molecular Imager
BioTek Synergy-2 Fluorometer
RNA Extraction
Price on request

Taueret Laboratories offers RNA extraction and quality control for a variety of sample types including:
• Whole Blood
• Buffy Coat
• Cells
• FFPE Tissue
• Tissue

Taueret Laboratories offers RNA extraction and quality control for a variety of sample types including:
• Whole Blood
• Buffy Coat
• Cells
• FFPE Tissue
• Tissue

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Whole blood
FFPE tissue
Frozen Tissue
cells
RNA Extraction
Buffy Coat
DNA/RNA Analysis and Quality Control
Price on request

Nano Drop
Pico
Gels

Nano Drop
Pico
Gels

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Automation Consulting
Price on request

Automation Services

Automation Services

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Clinical Research
Price on request

Clinical Research Services

Clinical Research Services

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Biospecimen Management and Storage
Price on request

DNA Sample Storage
WBC Sample Storage
Tissue Sample Storage
Data Storage

DNA Sample Storage
WBC Sample Storage
Tissue Sample Storage
Data Storage

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Project Management, Consulting, & Support Services
Price on request
Request a quote for more information about this service.
Targeted Gene Sequencing
Price on request

Targeted Gene Sequencing Services

Targeted Gene Sequencing Services

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2018-06-21 06:35:40 -1100

Net Promoter Score of 10 received for DNA Extraction.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.

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