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Blog

Alternative To Blood Samples Exome Sequencing Screening

November 7, 2023

In a study published by the NPJ Genomic Medicine, Three young children presented with a neurodevelopmental disorder were studied to identify if there were pathogenic variants found in their ATG4D bi-allele. Instead of blood samples, oral DNA samples were collected from two of the three participants and…

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Featured articles

iSWAB Microbiome Collection Media:
January 12, 2022

iSWAB Microbiome Collection Media: Supporting Home Collection…

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Mawi DNA Technologies Supports
October 25, 2021

Mawi DNA Technologies Supports UC San Diego…

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Mawi DNA Technologies
October 4, 2021

Mawi DNA Technologies Announces distribution agreement with…

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Conservation Organization
August 19, 2021

Genetic Database Collection for Turtle Species: Mawi…

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Enabling Faster, Higher Throughput COVID-19
November 3, 2020

Enabling Faster, Higher Throughput COVID-19 Testing and…

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We asked ChatGPT
April 21, 2023

We asked ChatGPT

Mawi Asked ChatGPT We asked an AI platform the following question Question: Why is bacterial DNA contamination not good for genomicDNA sequencing? Answer: Bacterial DNA contamination can interfere with genomic DNA sequencing in several ways, making it less accurate and reliable.   Here are some…

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Abstract biology
April 17, 2023

Candida Data Using iSWAB In Response to New Infectious Diseases

A deadly fungal infection, Candida Auris, is becoming a serious threat. This drug-resistant strain is deadly for those with weakened immune systems and is spreading at an alarming rate. The iSWAB-Microbiome-EL has been proven to safely collect and transport samples suspected of containing the infection and has…

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Medical research and chemistry looking to cure diseases
April 11, 2023

Top Reasons to Ditch Your Current VTM. Upgrade your Viral Transport Media

Mawi DNA has developed iSWAB-RC-EL, an FDA approved sample collection device for transport and storage of samples suspected of containing an infectious disease*. Why iSWAB-RC-EL is the superior option: 1. FDA Approved* 2. Skip the RNA extraction step in PCR workflow 3. Inactivates viruses and other…

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More news

November 19, 2019

The Mawi DNA Story – “Out of pain comes resolve”

In the video above, Dr. El-Fahmawi shares a personal experience of his child having serious ailments as a baby. She was severely ill and doctors had a difficult time diagnosing the issue. Going through the traumatic experience resulted in the creation of the company, Mawi DNA. Dr. El-Fahmawi saw that…

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November 5, 2019

Spit DNA Collection Limitations Magnifies Genomics Research Diversity Issue

We have been advocating that the diversity in genomics research is an issue since Mawi DNA’s inception in 2014. Interestingly, in late 2018 and now 2019 several publications came out to describe this issue in greater details.   Unfortunately, such gap of genetic data hinders progress…

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October 22, 2019

Automation-Friendly RNA Purification Chemistry for Mawi iSWAB-RNA-v2 by MAGBIO Genomics

Click here for the link to the full article. Supporting Data: RNA-Extraction-from-iSWAB-RNA-v2-with-HighPrep

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October 15, 2019

Why do we give so much blood?

Almost everyone has provided a blood sample at a certain point of life, but ever wondered why so many tubes? How Blood Samples Are Taken Using current analytical technologies, several health indicators/analytes can only be obtained from blood and therefore giving a blood sample is…

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October 14, 2019

De Novo SIX1 Variant and Nonsyndromic Cochleovestibular Nerve Abnormality

Abstract Background: Childhood hearing impairment affects language and cognitive development. Profound congenital sensorineural hearing impairment can be due to an abnormal cochleovestibular nerve (CVN) and cochleovestibular malformations, however, the etiology of these conditions remains unclear. Methods: We used a trio‐based exome sequencing approach to unravel…

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July 30, 2019

Pleiotropic Effects in Exome Sequencing of Siblings with Autism Spectrum Disorder and Speech Sound Disorder

Article Abstract Recent studies of autism spectrum disorder (ASD) and childhood apraxia of speech (CAS) have resulted in conflicting conclusions regarding the comorbidity of these disorders on phenotypic grounds. In a nuclear family with two dually affected and one unaffected offspring, whole-exome sequences were evaluated…

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