Tests we offer
All testing performed or developed at Atlas is selected and validated in adherence with the highest clinical laboratory standards. We have a responsibility to our patients and clients to ensure our testing is accurate and reliable, and that our ordering and resulting process is secure and efficient for both patients and providers.
Carrier Screening
Full Panel
Our carrier screening panel looks for DNA mutations associated with over 100 diseases that can help predict the chances of having a child with a genetic disorder such as Cystic Fibrosis; Spinal Muscular Atrophy (SMA); Fragile X; Ashkenazi Jewish Screen; Tay-Sachs and many others.
- Full List – Carrier Screening
- ABCC8-related Hyperinsulinism
Achromatopsia
Alkaptonuria
Alpha-1 Antirypsin Deficiency
Alpha-Mannosidosis
Andermann Syndrome
ARSACS
Aspartylglycosaminuria
Ataxia With Vitamin E Deficiency
Ataxia-Telangiectasia
Autosomal Recessive Polycystic Kidney Disease
Bardet-Biedl Syndrome, BBS1-related
Bardet-Biedl Syndrome, BBS10-related
Biotinidase Deficiency
Bloom Syndrome
Canavan disease
Carnitine Palmitoyltransferase IA Deficiency
Carnitine Palmitoyltransferase II Deficiency
Cartilage-Hair Hypoplasia
Citrullinemia Type 1
CLN3-related neuronal Ceroid Lipofuscinosis
CLN5-related neuronal Ceroid Lipofuscinosis
Cohen Syndrome
Congenital Disorder of Glycosylation Type Ia
Congenital Disorder of Glycosylation Type Ib
Congenital Finnish Nephrosis
Costeff Optic Atrophy Syndrome
Cystic Fibrosis
Cystinosis
D-Bifunctional Protein Deficiency
Factor XI Deficiency
Familial Dysautonomia
Familial Mediterranean Fever
Fanconi Anemia Type C
Galactosemia
Gaucher Disease
GJB2-related DFNB1 Nonsyndromic Hearing Loss and Deafness - Glutaric Acidemia Type 1
Glycogen Storage Disease Type Ia
Glycogen Storage Disease Type Ib
Glycogen Storage Disease Type III
Glycogen Storage Disease Type V
GRACILE Syndrome
Hb Beta Chain-related Hemoglobinopathy (Including Beta Thalassemia and Sickle Cell Disease)
Hereditary Fructose Intolerance
Hereditary Thymine-Uraciluria
Herlitz Junctional Epidermolysis Bullosa, LAMA3-related
Herlitz Junctional Epidermolysis Bullosa, LAMB3-related
Herlitz Junctional Epidermolysis Bullosa, LAMC2-related
Hexosaminidase A Deficiency (Including Tay-Sachs Disease)
Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency
Hurler Syndrome
Hypophosphatasia, Autosomal Recessive
Inclusion Body Myopathy 2
Isovaleric Acidemia
Joubert Syndrome 2
Krabbe Disease
Limb-Girdle Muscular Dystrophy Type 2D
Limb-Girdle Muscular Dystrophy Type 2E
Lipoamide Dehydrogenase Deficiency
Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
Maple Syrup Urine Disease Type 1B
Medium Chain Acyl-CoA Dehydrogenase Deficiency
Megalencephalic Leukoencephalopathy With Subcortical Cysts
Metachromatic Leukodystrophy - Mucolipidosis IV
Muscle-Eye-Brain Disease
NEB-related Nemaline Myopathy
Niemann-Pick Disease Type C
Niemann-Pick Disease, SMPD1-associated
Nijmegen Breakage Syndrome
Northern Epilepsy
Pendred Syndrome
PEX1-related Zellweger Syndrome Spectrum
Phenylalanine Hydroxylase Deficiency
Polyglandular Autoimmune Syndrome Type 1
Pompe Disease
PPT1-related Neuronal Ceroid Lipofuscinosis
Primary Carnitine Deficiency
Primary Hyperoxaluria Type 1
Primary Hyperoxaluria Type 2
PROP1-related Combined Pituitary Hormone Deficiency
Pseudocholinesterase Deficiency
Pycnodysostosis
Rhizomelic Chondrodysplasia Punctata Type 1
Salla Disease
Segawa Syndrome
Short Chain Acyl-CoA Dehydrogenase Deficiency
Sjogren-Larsson Syndrome
Smith-Lemli-Opitz Syndrome
Steroid-Resistant Nephrotic Syndrome
Sulfate Transporter-Related Osteochondrodysplasia
TPP1-related Neuronal Ceroid Lipofuscinosis
Tyrosinemia Type I
Usher Syndrome Type 1F
Usher Syndrome Type 3
Very Long Chain Acyl-CoA Dehydrogenase Deficiency
Wilson Disease
Spinal Muscular Atrophy
Fragile X Syndrome
Atlas Express Panel
Targeted Sequencing is used to analyze specific gene regions associated with autosomal recessive inherited diseases.
- Full List – Atlas Express Panel
- Cystic Fibrosis
Spinal Muscular Atrophy
Fragile X
Tay-Sachs Disease
Sickle Cell Anemia
Alpha and Beta Thalassemia
Ashkenazi Jewish Screening
Ashkenazi Jewish genetic diseases are a group of rare disorders that occur more often in people of Eastern European (Ashkenazi) Jewish heritage than in the general population. Even though most of these diseases are severe and can cause early death, some can be treated to reduce symptoms and prolong life.
- Full List – Ashkenazi Jewish Screening
- Canavan Disease Familial Dysautonomia
- Maple Syrup Urine Mucolipidosis Type V
- Bloom Syndrome Niemann-Pick Disease Type A
- Cystic Fibrosis Spinal Muscular Atrophy
- Fanconi Anemia Familial Hyperinsulinism
- Glycogen Storage Disease 1A Nemaline Myopathy
- Gaucher Disease Usher IF and III
- Tay-Sachs Disease Joubert Syndrome Type 2
- Lipoamide Dehydrogenase Deficiency
CMX Panel
Targeted Sequencing is used to analyze specific gene regions associated with autosomal recessive inherited diseases.
- Full List – CMX Panel
- Cystic Fibrosis
Spinal Muscular Atrophy
Fragile X
Specialty Testing
UTI (Urinary Tract Infection) Screening / Antibiotic Resistance Testing
Real-time polymerase chain reaction assay to detect up to 25 pathogens, including bacterial, viral, and fungal infections
* Quick turnaround time of 48-72 hours
* Small sample size of 2mL
* Accurately treat UTIs the first time
* 100% specificity
* Easy-to-read one-page report
Antibiotic resistance addressed – targeted detection of resistance genes, spanning across 8 antibiotic classes
* Genotypes bacterial pathogens to reduce antibiotic resistance
- Full List – UTI Screenings
- Candida spp.
Enterobacter spp.
Enterococcus spp.
Citrobacter freundii
Escherichia coli
Klebsiella pneumoniae
Proteus mirabilis
Proteus vulgaris
Pseudomonas aeruginosa
Cytomegalovirus (CMV, Human Herpesvirus-5)
Staphylococcus saprophyticus
Streptococcus algalactiae (Group B)
Staphylococcus aureus
Acinetobacter baumannii
Chlamydia trachomatis
Gardnerella vaginalis
Neisseria gonorrhoeae
Trichomonas vaginalis
Herpes simplex virus 1 & 2 probes (HSV-1, HSV-2)
- Full List – Antibiotic Resistance Screenings
- VanA, VanB
mecA
ermB, C; mefA
qnrA2
tetM
SHV, KPC groups
CTX-M1 (15), M2 (2), M9 (9), M8/25 groups
IMP, NDM, VIM groups
OXA-48, -51
PER-1/VEB-1/GES-1 groups
dfr (A1, A5), sul (1,2) probes
Infectious Wound Screening / Antibiotic Resistance Testing
Detects the bacterial, fungal, and viral organisms known to be associated with wound and lesion infections. Antibiotic resistance addressed – targeted detection of resistance genes. *Denotes Nail Fungal Profile
- Full List – Infectious Wound Screening
- Antibiotic Resistance Testing
- Acinetobacter baumannii Proteus mirabilis
Anaerococcus vaginalis Proteus vulgaris
Bacteroides fragilis Pseudomonas aeruginosa
Burkholderia spp. Salmonella enterica
Citrobacter freundii Serratia marcescens
Clostridium spp. Staphylococcus aureus
Corynebacterium spp. Staphylococcus spp.
Enterobacter spp. Streptococcus pyogenes (Group A)
Escherichia coli Streptococcus agalactiae (Group B)
Enterococcus spp. Vibrio spp.
Finegoldia magna * Candida spp.
Fusobacterium spp. * Aspergillus spp.
Haemophilus influenzae * Blastomyces dermatitidis
Klebsiella spp. * Cladosporium spp.
Mycoplasma spp. * Curvularia spp., lunata
Peptoniphilus spp. * Epidermophyton floccosum
Peptostreptococcus spp. * Fusarim spp.
Propionibacterium spp., acnes * Malassezia spp.
* Microsporum spp.
- VanA, VanB
mecA
ermB, C; mefA
qnrA2
tetM
SHV, KPC groups - CTX-M1 (15), M2 (2), M9 (9), M8/25 groups
IMP, NDM, VIM groups
OXA-48, -51
PER-1/VEB-1/GES-1 groups
dfr (A1, A5), sul (1,2) probes
Women’s Health Screening
Screening of cervical cells to detect potentially pre-cancerous and cancerous processes in the cervix, as well as organisms associated with infection.
- Full List – Women’s Health Screening
- Pap, liquid-based
HPV Plus
Chlamydia trachomatis
Neisseria gonorrhoeae
Trichomonas vaginalis
Ureaplasma spp.
Mycoplasma genitalium
Atopobium vaginae
Megasphaera Type-1
Megasphaera Type-2
Lactobacillus spp.
Mobiluncus spp.
BVAB2
Gardnerella vaginalis - Herpes simplex 1
Herpes simplex 2
Treponema Pallidum
Lymphogranuloma venereum
Cytomegalovirus (CMV)
Varicella Zoster
Group B Strep
Candida spp.
Mycoplasma spp.
Pap, liquid-based (reflex to HPV Plus when ASC-US
COVID-19 Testing
- COVID-19 Testing
View Atlas’s COVID-19 Testing Information
NIPT (Non-Invasive Prenatal Testing)
Nucleic acid extraction from maternal blood for DNA sequencing and analysis of sequencing results to determine fetal aneuplody.
- Full List – NIPT Screening
- Chromosomes 21, 18, 13
- Sex Chromosome aneuploidies option
- Trisomies 9 and 16 option
- Microdeletions, including:
- 22q11 deletion (DiGeorge)
- 15q11 deletion (Angelman / Prader Willi)
- 1p36 deletion
- 4p- (Wolf-Hirschhorn)
- 5p- (Cri-du-chat)
About us
Contact Us
Hours
Mon – Friday 7:30 AM – 11:00 PM
Sat – Sun Closed / By Appointment Only
Phone
Phone: 888-618-9107 Ext: 1
Fax: 888-965-1390