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Next generation sequencing in the diagnostic approach to autosomal dominant polycystic kidney disease

• Authors : Braždžiūnaitė, Deimantė; Miglinas, Marius; Utkus, Algirdas

Subjects: autosomal dominant polycystic kidney; PKD1; PKD2

• Source: ESHG 2021: virtual conference, August 28-31, European Society of Human Genetics, 2021, p. [1]

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Microbial diversity during composting of the biomaterial waste as revealed by next-generation sequencing

• Authors : Vasiliauskienė, Dovilė; Biyada, Saloua; Merzouki, Mohammed

Subjects: biomaterial; next generation sequencing; textile waste

• Source: FEMS Online Conference on Microbiology, 28–31 October 2020 : Electronic abstract book, Belgrade : Federation of European Microbiological Societies (FEMS) with the Serbian Society of Microbiology

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Ethnicity-related DMD genotype landscapes in European and non-European countries

• Authors : Selvatici, Rita; Rossi, Rachele; Fortunato, Fernanda

Subjects: DMD; Duchenne muscular dystrophy; next-generation sequencing

• Source: Neurology genetics, Philadelphia : Lippincot Williams & Wilkins, 2021, vol. 7, iss. 1, art. no. e536, p. [1-12] ; ISSN 2376-7839

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One test for all: whole exome sequencing signifcantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome

• Authors : Meyer, Robert; Begemann, Matthias; Hübner, Christian Thomas

Subjects: Silver–Russell syndrome; next generation sequencing; diagnostic detection rate

• Source: Orphanet journal of rare diseases, London : BioMed Central Ltd., 2021, vol. 16, art. no. 42, p. [1-10] ; eISSN 1750-1172

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Evolution of microbial composition and enzymatic activities during the composting of textile waste

• Authors : Biyada, Saloua; Merzouki, Mohammed; Dėmčėnko, Taisija

Subjects: composting; organic waste; alkaline phosphatase

• Source: Applied sciences, Basel : MDPI AG, 2020, vol. 10, iss. 11, art. no. 3758, p. 1-26 ; ISSN 2076-3417

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Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice

• Authors : Tumienė, Birutė; Maver, A.; Writzl, K.

Subjects: diagnostic yield; epilepsy genetics; monogenic epilepsies

• Source: Clinical genetics, Hoboken : Wiley-Blackwell Publishing, Inc., 2018, vol. 93, p. 1057-1062 ; ISSN 0009-9163 ; eISSN 1399-0004

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Galaxy in teaching computational methods of genome analysis for master degree students in Medical Genetics program at the Faculty of Medicine, Vilnius University

• Authors : Pranckevičienė, Erinija; Ambrozaitytė, Laima; Uktverytė, Ingrida

Subjects: Galaxy; medical genetics; next generation sequencing

• Source: Galaxy Community Conference 2015, 6-8th July 2015, Norwich, UK : posters, Norwich, 2015, Art. No. P05

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Suaugusiųjų ūminės limfoleukemijos genominių veiksnių ir jų evoliucijos tyrimas ; Genomic aberrations and their evolution in adult acute lymphoblastic leukemi

• Authors : Dirsė, Vaidas; Griškevičius, Laimonas

Subjects: acute lymphoblastic leukemia; SNP array; next generation sequencing

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Genomic aberrations and their evolution in adult acute lymphoblastic leukemia ; Suaugusiųjų ūminės limfoleukemijos genominių veiksnių ir jų evoliucijos tyrimas

• Authors : Dirsė, Vaidas; Griškevičius, Laimonas

Subjects: acute lymphoblastic leukemia; SNP array; next generation sequencing

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Diversity analysis of pathogenic genomic variants and genes that cause the autosomal recessive diseases using whole exome sequencing ; Patogeninių genomo variantų ir jų genų, lemiančių autosomines recesyviąsias ligas, įvairovės analizė, panaudojant viso egzomo sekoskaitą

• Authors : Rančelis, Tautvydas; Kučinskas, Vaidutis

Subjects: Exome sequencing; next generation sequencing pipeline; ClinVar

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