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NEW YORK (GenomeWeb) – Over the last few years, noninvasive prenatal testing has been established for fetal chromosomal aneuploidy screening as well as to look for subchromosomal aberrations, such as microdeletions and microduplications. However, when the mother unwittingly carries a chromosomal or subchromosomal abnormality herself, many types of NIPT that rely on counting DNA molecules cannot tell whether the fetus has inherited it as well.

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In Cell this week: proteomic, genomic, and transcriptomic analysis of endometrial cancer; deep neural network learning-based approach to antibiotic discovery; and more.

Mar
18
Sponsored by
Roche

This webinar will discuss data from a recent real-world comparison study evaluating performance of two cell-free DNA methodologies as first-line prenatal screens.

Mar
31
Sponsored by
Isoplexis

This webinar will discuss the application of single-cell proteomics and immune-imaging in adoptive cell therapy (ACT) for cancer.