nextseqtm 500 massively parallel sequencing platform (Illumina Inc)
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Illumina Inc
nextseqtm 500 massively parallel sequencing platform
Nextseqtm 500 Massively Parallel Sequencing Platform, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 99/100, based on 9689 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nextseqtm+500+massively+parallel+sequencing+platform/NextSeq+500+to+NextSeq+550+Upgrade/pm38456993-58-8-14
Average 99 stars, based on 9689 article reviews
Nextseqtm 500 Massively Parallel Sequencing Platform, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 99/100, based on 9689 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nextseqtm+500+massively+parallel+sequencing+platform/NextSeq+500+to+NextSeq+550+Upgrade/pm38456993-58-8-14
Average 99 stars, based on 9689 article reviews
nextseqtm 500 massively parallel sequencing platform - by Bioz Stars,
2026-09
99/100 stars
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Related Articles
Sequencing:Article Title: Functional studies associate novel DUOX2 gene variants detected in heterozygosity to Crohn's disease. Article Snippet: 1 Department of Biology and Medical Genetics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czech Republic 2 PRENET Laboratoře Lékařské Genetiky s.r.o., Pardubice, Czech Republic 3 Institute of Molecular Genetics, Czech Academy of Sciences, Prague, Czech Republic 4 Department of Pediatric Hematology and Oncology, 2nd Medical Faculty, Childhood Leukaemia Investigation Prague, Charles University and Motol University Hospital, Prague, Czech Republic 5 Department of Pediatrics, 2nd Medical Faculty, Charles University and University Hospital Motol, Prague, Czech Republic Abstract Purpose Crohn’s disease is a chronic gastrointestinal inflammatory disease with possible extraintestinal symptoms.. There are predisposing genetic factors and even monogenic variants of the disorder.. One of the possible genetic factors are variants of the DUOX2 gene. |