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myGenomics (CLIA Compliant)

ic 8.8/10 Overall Rating 88% Positive
ic 38 Orders Completed
Alpharetta, Georgia, US

About myGenomics (CLIA Compliant)

Founded: 2014 Type: Privately Held Size: 1-10 employees

myGenomics, located in Alpharetta, GA, offers Next Generation Sequencing services on the Illumina platform as well as library preparation and Sanger sequencing services. Our team of scientists each have more than fifteen years of expertise in the field and can provide consultation to help design your NGS... Show more »

myGenomics, located in Alpharetta, GA, offers Next Generation Sequencing services on the Illumina platform as well as library preparation and Sanger sequencing services. Our team of scientists each have more than fifteen years of expertise in the field and can provide consultation to help design your NGS project in the most efficient way possible.

Specializing in custom target sequencing, whole genome sequencing, and RNA-seq, myGenomics has the expertise and resources to make your projects a success. Our dedicated team will provide you and your project focused attention, utilizing the best approach to provide high quality results with quickest turnaround time and best price in the industry.

Certifications:
NPI# 1720403116
CLIA# 11D2084528

Standard shipping requests:
- DNA, Blood, Saliva samples to be shipped in Blue Ice Packs.
- RNA, Tissue, Cells should be shipped in dry ice.

• All of myGenomics services are for Research Use Only. Not for Use in Diagnostic or Treatment Procedures.

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Certifications & Qualifications

Agilent Service Provider CLIA/CAP

Diversity Certificates

Minority owned business Woman owned small business

Our Services (113)


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Whole Genome Sequencing

Price on request

Turn-around 10-20days. No minimum sample requirement.
$3.000: 30-40G data sufficient to cover human genome 10-12x.
$6,000: 90-120G data sufficient to cover human genome 30-45x.

Initial sample QC, Illumina indexed library preparation and paired-end sequencing using the NextSeq v2 platform. Delivery of FASTQ data files via... Show more »

Turn-around 10-20days. No minimum sample requirement.
$3.000: 30-40G data sufficient to cover human genome 10-12x.
$6,000: 90-120G data sufficient to cover human genome 30-45x.

Initial sample QC, Illumina indexed library preparation and paired-end sequencing using the NextSeq v2 platform. Delivery of FASTQ data files via cloud.

Data analysis if needed is available for $15/Gb and will deliver VCF (variant call file) with BWA mapping and GATK variant call information. Included filters are variant allele frequency (1000 genome), known pathogenic variants (dbSNP) and suspect variants (frameshift, stop gain, stop loss), SIFT score, Polyphen score. Additional deliverables include: initial sample QC, fragmentation QC, library prep QC, sequencing reads QC, coverage and FastQC plots.

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Illumina NextSeq 500 sequencing system Human

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Whole Exome Sequencing (WES)

Price on request

Turn-around 10-20 business days. No minimum sample requirement.
Price includes: initial sample QC and indexed Illumina library preparation with capture using Agilent SureSelect AllExon v6. ~50X coverage (5G) generated using paired-end reads sufficient to cover 80% exons >20x. Delivery of FASTQ data. Data analysis available for $15/Gb.

Turn-around 10-20 business days. No minimum sample requirement.
Price includes: initial sample QC and indexed Illumina library preparation with capture using Agilent SureSelect AllExon v6. ~50X coverage (5G) generated using paired-end reads sufficient to cover 80% exons >20x. Delivery of FASTQ data. Data analysis available for $15/Gb.

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Illumina HiSeq 2500 Illumina NextSeq 500 sequencing system Human Dog Cow Agilent SureSelect Show 6 more tags Show less

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Targeted Exome Sequencing

Price on request

The Agilent SureSelect Focused Exome design is highly targeted panel that enables deep coverage of only those regions within the human genome that have been associated with disease, allowing you to focus on mutations that matter.

5,000 Disease Associated Genes; 100x coverage; 95% targets covered > 20x

Service... Show more »

The Agilent SureSelect Focused Exome design is highly targeted panel that enables deep coverage of only those regions within the human genome that have been associated with disease, allowing you to focus on mutations that matter.

>5,000 Disease Associated Genes; 100x coverage; 95% targets covered > 20x

Service includes:
Initial sample QC on Nanodrop, Qubit and visualization through agarose gel electrophoresis.
Illumina Iibrary preparation, library QC
Agilent SureSelect Focused Exome capture, capture QC
Paired-end sequencing on Illumina NextSeq, FastQC
1.5G ± 0.15 data per sample

Project Details:
Customer submitted gDNA: >2ug; min. 25ng/ul;
Data will be delivered via Google Drive/Base Space as unanalyzed FASTQ files unless data analysis requested for additional $50/sample.

Turnaround time:
For acceptable samples, turn around time for delivery of FASTQ files is 10-20 days from initial QC of sample.

No minimum sample volume requirement.

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Agilent SureSelect Focused Exome Agilent SureSelect

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Targeted Genomic Enrichment

Price on request

OneSeq - One assay for genome-wide CNV, LOH, Mutations, SNPs, InDels:

Agilent's OneSeq target enrichment panel is revolutionizing cytogenetic research by providing one assay for wide spectrum of genetic variations in Constitutional Diseases (e.g. monogenic disorders, developmental disorders, intellectual disabilities) allowing... Show more »

OneSeq - One assay for genome-wide CNV, LOH, Mutations, SNPs, InDels:

Agilent's OneSeq target enrichment panel is revolutionizing cytogenetic research by providing one assay for wide spectrum of genetic variations in Constitutional Diseases (e.g. monogenic disorders, developmental disorders, intellectual disabilities) allowing to:
Detect copy number changes at a targeted resolution of 300kb in a genome-wide backbone
Detect copy number changes at a targeted higher resolution of 25kb– 50kb in disease-associated ClinGen regions
Detect genome-wide LOH as small as 5Mb
Detect mutations, SNPs and InDels

Sample to data in 20-30days. Data analysis if needed is available at $200/sample.

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Illumina HiSeq 2500 Illumina NextSeq 500 sequencing system Human Agilent SureSelect XT Human All Exon v5 Agilent SureSelect Focused Exome Agilent OneSeq Show 6 more tags Show less

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Whole Genome Assembly

Price on request

NGS technologies are able to provide high genome coverages at a relatively low cost. However, due to limited read length, de novo assembly often leaves gaps or fails to distinguish circular genomes from linear. myGenomics can fill this gap by combining standard library prep (PE100) with a single (3-5Kb) mate-pair library followed... Show more »

NGS technologies are able to provide high genome coverages at a relatively low cost. However, due to limited read length, de novo assembly often leaves gaps or fails to distinguish circular genomes from linear. myGenomics can fill this gap by combining standard library prep (PE100) with a single (3-5Kb) mate-pair library followed by sequencing at high depth coverage for Whole Genome Sequencing. The mean sequencing depth coverage for this service is >100x for smaller genomes (up to 5Mb). Sequencing is performed on an Illumina platform and data analysis delivering assembled genome (FASTa file) is included. 2-5 micrograms of single species specific purified DNA required.

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Illumina HiSeq 2500 Illumina MiSeq Bacteria

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RNA Sequencing

Price on request

$450/sample for 20million paired end 75 reads on illumina NextSeq. Turn-around 10-20days from sample received to FASTq data delivered. No minimum sample requirement.

Data analysis $100/sample will include:
Gene expression report, FPKM values (TopHat),
Differential gene expression report comparing samples (CuffDiff),
Single... Show more »

$450/sample for 20million paired end 75 reads on illumina NextSeq. Turn-around 10-20days from sample received to FASTq data delivered. No minimum sample requirement.

Data analysis $100/sample will include:
Gene expression report, FPKM values (TopHat),
Differential gene expression report comparing samples (CuffDiff),
Single Nucleotide Variation discovery
Fusion Gene Detection
Turn around time for analysis: 1 week
Pathway identification (additional price)

Additional deliverables
Initial sample QC, cDNA Library prep QC, Fragmentation QC, Sequencing reads QC, Coverage and FastQC plots.

RNA-seq can provide a profile of RNA presence, quantity, and sequence at a given moment in time or under specific conditions. Applications include:
- Gene Expression, identification of alternative gene spliced transcripts
- Differential Gene Expression comparing control and test conditions for example
- Pathway analysis to identify metabolic pathways affected under test conditions
- Single Nucleotide Variation Discovery
- Post Transcriptional Variations
- Fusion Gene Detection
- Transcriptome assembly of novel genomes

We offer a variety of services to best meet your budget and experimental needs.
Universal RNA-seq: Strand specific sequencing which includes polyA, long non-coding RNA, non-adenylated RNA, smRNA.

PolyA RNA-seq: Selective enrichment of poly-adenylated transcripts for cDNA preparation. Strand bias is not conserved.

Whole Transcriptome: Selective depletion of rRNA is followed by cDNA preparation allowing detection of lncRNA as well as mRNA. Strand bias is not conserved.​

Strand-specific library preparation: ​Ligation of unique adapters to the 5'- and 3'-ends of RNA fragments allows discrimination of the template DNA strand. This can be applied to either polyA or whole transcriptome projects.​​​

smRNA-seq/miRNA-Seq: Similar to strand-specific library preparation, with size selection to limit insert size of 19-21nt.

Normalized libraries: Treated with duplex-specific nuclease (DSN), resulting in under-representation of highly expressed transcripts, allowing detection of less abundant transcripts. Not suitable for experiments that need to retain expression profiling information.

Custom Target RNA-Seq: ​Please inquire with a list of target of interest.

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Illumina NextSeq 500 sequencing system Tophat Cuffdiff

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Illumina Sequencing

Price on request

myProfile:
Whole Genome
Whole Exome
Focused Exome (5,600 disease associated genes)
Whole Transcriptome (RNA-Seq)
​myBiome: Metagenomics
ChIP-Seq​

Cancer Genomics:
Breast, Ovarian, Prostate, Lung, Liver, Colorectal
Cancer HotSpots & Comprehensive testing

Gene Panels:
myMedAct Panel (57... Show more »

myProfile:
Whole Genome
Whole Exome
Focused Exome (5,600 disease associated genes)
Whole Transcriptome (RNA-Seq)
​myBiome: Metagenomics
ChIP-Seq​

Cancer Genomics:
Breast, Ovarian, Prostate, Lung, Liver, Colorectal
Cancer HotSpots & Comprehensive testing

Gene Panels:
myMedAct Panel (57 Clinically actionable genes)
myRxAct Panel (Drug metabolism genes)
Hereditary Inclusion Body Myopathy Panel
Custom Targets

SNP Genotyping:
Apolipoprotein E, Factor V Leiden, ​Prothrombin ​

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Illumina HiSeq 2500 Illumina MiSeq MiSeq FGx Forensic Genomics System Human Dog Cow Show 6 more tags Show less

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Breast Cancer Gene Panel

Price on request

Turn-around 10-12days from sample received to data delivered. No minimum sample requirement. Price includes initial sample QC and indexed Illumina library preparation with capture and sequencing of BRCA1 and BRCA2 genes. ~100X coverage generated using paired-end reads. Delivery of FASTQ data. Analysis available for $50/sample. DNA... Show more »

Turn-around 10-12days from sample received to data delivered. No minimum sample requirement. Price includes initial sample QC and indexed Illumina library preparation with capture and sequencing of BRCA1 and BRCA2 genes. ~100X coverage generated using paired-end reads. Delivery of FASTQ data. Analysis available for $50/sample. DNA extraction available for $20/sample. Bulk order discounts available.

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Illumina HiSeq 2500 Illumina MiSeq Human

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Targeted Cancer Gene Panel

Price on request

Initial sample QC and cancer hotspot exome sequencing using Illumina'sTrueSeq Cancer Kit. 0.15G of data generated using NextSeq paired-end reads (>100X).  Delivery of FASTQ data.  Analysis available, please inquire. 

Initial sample QC and cancer hotspot exome sequencing using Illumina'sTrueSeq Cancer Kit. 0.15G of data generated using NextSeq paired-end reads (>100X).  Delivery of FASTQ data.  Analysis available, please inquire. 

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Illumina HiSeq 2500 Illumina MiSeq Illumina NextSeq 500 sequencing system Human

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DNA/RNA Analysis and Quality Control

Price on request

Quantification of DNA and RNA using Agilent screen tape and Tapestation.
Genomic DNA: $10/sample
High Sensitive DNA: $10/sample
High Sensitive RNA: $10/sample
Min. 10 samples. QC report delivered through email.

Quantification of DNA and RNA using Agilent screen tape and Tapestation.
Genomic DNA: $10/sample
High Sensitive DNA: $10/sample
High Sensitive RNA: $10/sample
Min. 10 samples. QC report delivered through email.

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Agilent Bioanalyzer Agilent TapeStation Human Mouse Rat Bacteria Dog Cow Show 8 more tags Show less

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DNA Quantification

Price on request

High sensitive DNA quantification using fluorescence based Qubit assay following manufacturer's instructions (Invitrogen). Min. 10 samples.

High sensitive DNA quantification using fluorescence based Qubit assay following manufacturer's instructions (Invitrogen). Min. 10 samples.

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Qubit 2.0 fluorometer

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Genomic DNA Extraction

Starting at $20.00 per sample

DNA extraction and QC from cells, body fluid, blood, saliva or tissue. Extraction from FFPE samples will be $40/sample.

DNA extraction and QC from cells, body fluid, blood, saliva or tissue. Extraction from FFPE samples will be $40/sample.

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Biomek Liquid Handling Robot Human Mouse

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Illumina NGS Library Preparation

Starting at $125.00 per library

Initial sample QC using Agarose gel electrophoresis, Nanodrop and Qubit assays.
DNA fragmentation on Bioruptor and QC on Tapestation.
Indexed Illumina library preparation and QC on Tapestation. Agilent Bravo liquid handler employed for high throughput library preparation. All QC reports delivered.

Initial sample QC using Agarose gel electrophoresis, Nanodrop and Qubit assays.
DNA fragmentation on Bioruptor and QC on Tapestation.
Indexed Illumina library preparation and QC on Tapestation. Agilent Bravo liquid handler employed for high throughput library preparation. All QC reports delivered.

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Agilent Bravo Human

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Inherited Disease Gene Panel

Price on request

Capture and analysis of coding regions of 57 medically advisable genes including UTRs, with QC reporting. ~100X coverage generated using MiSeq paired-end 100nt reads. Delivery of FASTQ data. Analysis available, please inquire. Turn-around <2 weeks.

Capture and analysis of coding regions of 57 medically advisable genes including UTRs, with QC reporting. ~100X coverage generated using MiSeq paired-end 100nt reads. Delivery of FASTQ data. Analysis available, please inquire. Turn-around <2 weeks.

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Human

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Multiplex Ligation-Dependent Probe Amplification (MLPA)

Starting at $100.00 per sample

MLPA BRCA analysis

Multiplex Ligation-dependent Probe Amplification detecting abnormal copy numbers of BRCA1 and BRCA2

MLPA BRCA analysis

Multiplex Ligation-dependent Probe Amplification detecting abnormal copy numbers of BRCA1 and BRCA2

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RNA Extraction and Purification

Starting at $50.00 per sample

Extraction of total RNA including small RNA from cells, blood or tissue and QC on tapestation including electropherogram, concentrations and RIN values.

Extraction of total RNA including small RNA from cells, blood or tissue and QC on tapestation including electropherogram, concentrations and RIN values.

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Sanger Sequencing

Price on request

Sanger sequencing of your target area. Customer to provide DNA and primers for target area. Sequence generated on ABI 3730XL. Insilico amplicon design and primer synthesis available.

Sanger sequencing of your target area. Customer to provide DNA and primers for target area. Sequence generated on ABI 3730XL. Insilico amplicon design and primer synthesis available.

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Shotgun Library Construction Service

Price on request

Initial sample QC and indexed Illumina library preparation. ChIP or genomic DNA accepted as input. No capture. Turn around <1 week.

Initial sample QC and indexed Illumina library preparation. ChIP or genomic DNA accepted as input. No capture. Turn around <1 week.

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Clinical Molecular Diagnostics

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Spectroscopy

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Computational Modeling

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Imaging & Spectroscopy

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Biostatistics & Bioinformatics

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Plasmid DNA Preparation

Price on request

Mini, Midi, Maxi preps with automation for consistent yield.

Mini, Midi, Maxi preps with automation for consistent yield.

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Gene Expression Analysis

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DNA Purification

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Statistical Analysis

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Spectrophotometry

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Regression Analysis

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Separation/Purification Services

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Protein Sequencing

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Biology

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PCR

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PCR Product Purification

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Next Generation Sequencing (NGS)

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Model Organisms

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Microarray Experimental Design

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DNA Libraries

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Gene Annotation

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Gel Electrophoresis

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ChIP-Seq Library Preparation

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Text Mining

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Targeted Sequencing

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Plasmid Sequencing

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Microarray Data Analysis

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Metagenomics

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Clinical Research

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Automated Liquid Handling

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High Performance Computing

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Genotyping and Gene Expression Assays

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Assay Development

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DNA Sequencing

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Nucleic Acid Data Analysis

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DNA Microarrays

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Exome Sequencing Services

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cDNA Synthesis

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Bioinformatics

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Agarose Gel Electrophoresis

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Clinical Laboratory Services

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Project Management

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Nucleic Acid Services

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DNA Services

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DNA Fragment Analysis

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Gene Panel Testing

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Chemistry and Materials

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Equipment

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DNA Synthesis and Probe Development

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Protein Services

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Biochemistry & Molecular Biology

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Targeted Gene Sequencing

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Analytical Chemistry Services

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Automation Consulting

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Sequencing Data Analysis and Management

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Plasmids and Vectors

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RNA Services

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DNA Library Preparation

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Animal Models and Studies

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DNA Extraction and Purification

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Electrophoresis

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Nucleic Acid Analysis

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Lead Identification and Validation

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Data Services

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Scientific Sourcing

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Gene Copy Number Analysis

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SNP Genotyping

Single Nucleotide Polymorphism Genotyping
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Transgenic Genotyping

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Drug Discovery & Development

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Microbiology

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Drug Discovery

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Cells and Tissues

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Biospecimens

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Genetic Marker Screening Services

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BRCA Mutation Analysis

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myMedAct Panel

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Compound Library Synthesis

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Infectious Disease Animal Models

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Drug Target Identification

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Bacterial Infection Animal Models

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Viral Infection Animal Models

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Genomics Data Analysis

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Microbiome Studies

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In Silico Next Generation Sequencing Analysis

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In Silico Metagenomics/Metatranscriptomics Analysis

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DNA Methylation Analysis

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MicroRNA (miRNA) Expression Profiling

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Restriction Fragment Length Polymorphism (RFLP) Analysis

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Error-Prone PCR

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Breast Cancer Human DNA

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Epigenetic Studies

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Human Biospecimens

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Human DNA and RNA Samples

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Animal Models of Disease

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Microbiology Assays

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  • Positive review for Illumina Sequencing:

    September 2016

    "My sequencing facility closed down and I was hesitant to go with anyone else. After failing with a MinION, I decided it was time to venture elsewhere. myGenomics offered up outstanding work, excellent communication, and fast turnaround. They completed the job within specs and sent the QC and data, it was easy stuff. I will be using them again. And no, I am not a computer, nor am I an employee of this company, I am a scientist and instructor. Look me up and send me an email if you have questions. Jeffery Hughey (Hartnell College)"

  • Positive review for Breast Cancer Gene Panel:

    April 2016

    "I think all was great! So fast!"

  • Positive review for DNA/RNA Analysis and Quality Control:

    April 2016

    "myGenomics provided a fair price, fast turnaround time and excellent service for our tape station project. We would definitely use them again."

  • Positive review for RNA Sequencing:

    April 2016

    "I was very happy with the results provided by myGenomics. The company went above and beyond the call of duty in some cases and was very patient with our difficult order. Results were excellent. We will use them again. We highly recommend! John A. Eimes Seoul National University"

  • Positive review for Whole Genome Sequencing:

    July 2014

    "We are satisfied with this lab and may use them to conduct more WGS work."

myGenomics (CLIA Compliant) has not received any endorsements.