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Affiliated Genetics, Inc.

Salt Lake City, Utah, US

Affiliated Genetics, Inc. (AGI), founded in April 1994, provides dozens of medical DNA testing applications and a full range of genomic services. Located in Salt Lake City, UT, the laboratory provides outstanding customer service with a highly trained staff of scientists, technicians and customer service representatives.

AGI’s scientists are recognized as experts in the genetics community and have published hundreds of scientific papers related to DNA testing. AGI voluntarily participates in proficiency testing programs and adheres to strict accreditation standards and practices of the CAP, CLIA, and AABB.

Dr. Kenneth Ward, M.D. - Laboratory Director, Medical Geneticist
Dr. Guity Gaffari, PhD - Assistant Laboratory Director, Medical Geneticist

Affiliated Genetics, Inc. has not listed any services.

Whole Exome Sequencing
Starting at $1,050.00 per sample

Affiliated Genetics is a CLIA, CAP, AABB accredited laboratory located in Salt Lake City, Utah since 1994.

Whole Exome Sequencing for research only. Standard output raw data to include VCF / BAM / BAI files only.

Mean depth coverage 100x
1-10 samples - $1,050
11-50 samples - $925
>50 samples - $800

Mean depth... Show more »

Affiliated Genetics is a CLIA, CAP, AABB accredited laboratory located in Salt Lake City, Utah since 1994.

Whole Exome Sequencing for research only. Standard output raw data to include VCF / BAM / BAI files only.

Mean depth coverage 100x
1-10 samples - $1,050
11-50 samples - $925
>50 samples - $800

Mean depth coverage 30x
1-10 samples - $725
11-50 samples - $650
>50 samples - $550

*Projects smaller than 50 samples will be run on the Ion Proton sequencing platform using Ion Hi-Q Chemistry and the P1V3 chip (see Life Technologies website for details). Projects larger than 50 samples may be run on the Illumina HiSeq 4000.

**Raw data plus custom initial Cartagenia filtering also available for an additional fee.

**Clinical Exome Sequencing with full interpretation is also available through Affiliated Genetics. Please call for details regarding pricing.

****TURN AROUND TIME FOR LESS THAN 50 SAMPLES 3 WEEKS

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Whole Genome Sequencing
Starting at $4,150.00 per sample

Affiliated Genetics is a CLIA, CAP, AABB accredited laboratory located in Salt Lake City, Utah since 1994.

Whole Genome Sequencing for research only. Standard output raw data to include VCF / BAM / BAI files only.

Mean depth coverage 90x
1-4 samples - $4,150 each
5-12 samples - $4,000 each
>12 samples - $3,750... Show more »

Affiliated Genetics is a CLIA, CAP, AABB accredited laboratory located in Salt Lake City, Utah since 1994.

Whole Genome Sequencing for research only. Standard output raw data to include VCF / BAM / BAI files only.

Mean depth coverage 90x
1-4 samples - $4,150 each
5-12 samples - $4,000 each
>12 samples - $3,750 each

Mean depth coverage 30x
1-4 samples - $3,000 each
5-12 samples - $2,850 each
>12 samples - $2,500 each

*All WGS samples will be run on the Illumina HiSeq 4000.

**Raw data plus custom initial Cartagenia filtering also available for an additional fee.

***WGS can be performed using a CLIA protocol when results are to be reported to patients with a full clinical interpretation. Please call for details regarding pricing.

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Affymetrix High Throughput (HT) Microarray
Starting at $65.00 per sample

Processing of samples using the Affymetrix Gene Titan instrument. Does not include price of array. Samples numbers must take into account optimal format of desired array.

Under 100 samples $65 each
100-499 samples $60 each
500-1000 samples $55 each
1001-5000 samples $50 each
Over 5000 samples $40 each

Processing of samples using the Affymetrix Gene Titan instrument. Does not include price of array. Samples numbers must take into account optimal format of desired array.

Under 100 samples $65 each
100-499 samples $60 each
500-1000 samples $55 each
1001-5000 samples $50 each
Over 5000 samples $40 each

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Affymetrix DNA microarray
Starting at $75.00 per sample

Processing of samples using the Affymetrix 3000 system. Does not include price of array.

Under 100 samples $75 each
100-499 samples $65 each

Turn around time for 100 samples or less - 3 weeks.

Processing of samples using the Affymetrix 3000 system. Does not include price of array.

Under 100 samples $75 each
100-499 samples $65 each

Turn around time for 100 samples or less - 3 weeks.

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Affymetrix GeneChip System 3000
Genomic DNA extraction
Starting at $22.00 per sample

Genomic DNA extraction for up to 6ml whole blood or 5ml saliva. Extraction includes three QC metrics. Concentrations of the samples are determined with spectrometry by measuring an A260 absorbance. An estimate of purity is determined by an A260/A280 ratio. Further QC will be performed by PicoGreen measurement and gel electrophoresis.

Volume discounts available.

Genomic DNA extraction for up to 6ml whole blood or 5ml saliva. Extraction includes three QC metrics. Concentrations of the samples are determined with spectrometry by measuring an A260 absorbance. An estimate of purity is determined by an A260/A280 ratio. Further QC will be performed by PicoGreen measurement and gel electrophoresis.

Volume discounts available.

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Twin Zygosity Testing
Starting at $150.00 per unit

Genotyping for the STR markers from the Promega PowerPlex-16 assay. Analysis of the assay will be performed via capillary electrophoresis using the Applied BioSystems 3130xl Genetic Analyzer. Genotypes for the twin pairs will be compared (Twin A vs. Twin B). If two or more markers are not concordant, the twins by default are... Show more »

Genotyping for the STR markers from the Promega PowerPlex-16 assay. Analysis of the assay will be performed via capillary electrophoresis using the Applied BioSystems 3130xl Genetic Analyzer. Genotypes for the twin pairs will be compared (Twin A vs. Twin B). If two or more markers are not concordant, the twins by default are Dyzygotic. If Twin A and Twin B are concordant for all markers analyzed, they are Monozygotic with greater than 99% probability.

Pricing includes both twin's samples. Includes DNA extraction for routine samples.

Volume discounts available.

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Fragile X Syndrome testing
Starting at $270.00 per sample

Fragile X Syndrome (FXS) is the most common genetic cause of intellectual disability (ID) and also the most common known genetic cause of autism or autism spectrum disorder1. Characteristics of FXS include speech and learning delays, behavioral differences such as autism-like behaviors, anxiety, and hyperactivity, as well as... Show more »

Fragile X Syndrome (FXS) is the most common genetic cause of intellectual disability (ID) and also the most common known genetic cause of autism or autism spectrum disorder1. Characteristics of FXS include speech and learning delays, behavioral differences such as autism-like behaviors, anxiety, and hyperactivity, as well as characteristic physical findings1,2. The condition is caused by a mutation in the FMR1 gene located on the X chromosome and follows an X-linked pattern of inheritance.

Clinical testing also available for physicians and their patients.
Reflex methylation Fragile X testing also available.

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Cystic Fibrosis Gene Panel
Starting at $710.00 per sample

Cystic Fibrosis-139 Variant Screen

The CF-139 panel is the largest FDA-cleared assay of clinically relevant mutations across diverse
demographics. The panel detects common CFTR mutations found in Caucasian, Ashkenazi Jewish, Hispanic, African American, Middle Eastern, Native American and Asian ethnicities using the illumina®... Show more »

Cystic Fibrosis-139 Variant Screen

The CF-139 panel is the largest FDA-cleared assay of clinically relevant mutations across diverse
demographics. The panel detects common CFTR mutations found in Caucasian, Ashkenazi Jewish, Hispanic, African American, Middle Eastern, Native American and Asian ethnicities using the illumina® MiSeqDx® platform. The CF-139 panel can be especially useful in individuals or couples of mixed or unknown ethnicities.

Clinical testing also available for physicians and their patients.
Discounted pricing for large sample volumes available.

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