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Archive

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Jan 13 / Roche
Roche KAPA HyperExome V2 in routine whole-exome sequencing
Christian Betz, Head of Molecular Genetics, R&D / NGS, at Bioscientia Human Genetics in Germany and presents on routine, automated whole exome sequencing clinical research workflows in human genetics applications.

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Jan 13 / Roche
Genetic newborn screening for rare diseases: The Screen4Care project
Alessandra Ferlini, Associate Professor in Medical Genetics, Head of the Medical Genetics Unit at the University of Ferrara, Italy, and Coordinator of the EU-IMI project, Screen4Care focused on genomic newborn screening and digital health presents an overview of the Screen4Care research project involving targeted NGS approaches and its potential impact on understanding rare genetic disorders in newborns.

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Dec 13 / Roche and Genentech
The global failure of mammography screening accessibility - a systematic literature review
Disparities in breast cancer (BC) outcomes between high-income and low-income countries result from social determinants and limited access to mammography screening, leading to later diagnoses and poorer prognoses. Understanding and addressing the barriers to BC care are critical for improving clinical outcomes and achieving the World Health Organization's 2021 Global Breast Cancer Initiative ambition (to reduce BC mortality by implementing early detection, timely diagnosis, and comprehensive BC management). This poster presents the findings from a systematic literature review of the barriers that women face in accessing mammography screening, diagnosis, and BC treatment. An estimation of the number of women worldwide affected by delays or lack of access to medical services is also reported.