Results 121 to 130 of about 29,122 (264)

Long‐read sequencing reveals SVA insertion in AP3B1 causing Hermansky–Pudlak syndrome 2

Pediatric Allergy and Immunology, Volume 37, Issue 7, July 2026.
Naomi Baba, Ahmed Elashy, Oliver Wegehaupt, Barbara Zieger, Melisa Felek, Micol Ferro, Kimberly Gilmour, Ute Fischer, Arndt Borkhardt, Stephan Ehl, David Koppstein, Sujal Ghosh   +11 more
wiley   +1 more source

VNTR Raw data

, 2014
This file contains the numbers of the repeats obtained from the sequenced VNTR loci. These data were implemented to generated the Minimum Spanning Network using BioNumerics software (version 7 ...
Anibal Tapiero (3314844), Nathalia Arias-Rojas (3314847), César A. Trujillo (3314853), César A. Medina (3314850), Bernal, Adriana J., Trujillo, César A., Medina, César A., Silvia Restrepo (204944), Adriana J. Bernal (662033), Lucie Poulin (488933), Koebnik, Ralf, Restrepo, Silvia, Poulin, Lucie, Tapiero, Anibal, Arias-Rojas, Nathalia, Ralf Koebnik (93571)   +15 more
core   +1 more source

Genotyping data (SNP & VNTR) obtained for burial GC96.

, 2015
Genotyping data (SNP & VNTR) obtained for burial GC96.
Sarah A. Inskip (738334), Simon A. Mays (738336), Graham R. Stewart (7103), Oona Y-C Lee (408404), Gurdyal S. Besra (37660), Houdini H. T. Wu (147464), Alistair W. G. Pike (408400), Gareth Llewellyn (738337), David E. Minnikin (147485), G. Michael Taylor (408398), Christopher M. Williams (254382), Sonia R. Zakrzewski (738335)   +11 more
core   +1 more source

Estimated haplotype frequencies for common haplotype blocks (≥1%) containing a given VNTR type.

, 2012
Haplotypes that included the VNTR were estimated in 322 Caucasian patients using the following marker alleles: rs1001761, VNTR, rs699517, rs3744962, rs9948583, rs495139, rs2298582, rs2298581, rs2471186, rs7236747, and rs2612092.
Alison P. Klein (173817), Roxann G. Ingersoll (173811), James R. Eshleman (173814), Soma Ghosh (173803), Michael G. Goggins (173808), Michael Borges (173805), Scott E. Kern (173820), M. Zulfiquer Hossain (173804)   +7 more
core   +1 more source

Variable number tandem repeat (VNTR) assay.

, 2013
Genomic DNA of ELC and DS1 cells were isolated and amplified by PCR for VNTR assay (top and bottom panels, respectively). The middle panel shows the VNTR of pre-mixed genomic DNA from both cells at 1∶1 ratio.
Kraig Abrams (387075), Wayne J. E. Lamm (387076), Robb W. Glenny (387077), Mineo Iwata (387073), Beverly Torok-Storb (235363), David K. Madtes (387074), Richard A. Nash (38132), Aravind Ramakrishnan (387078)   +7 more
core   +1 more source

Primer sequence for each VNTR marker amplified by nested PCR.

, 2015
Primer sequence for each VNTR marker amplified by nested PCR.
Yann Reynaud (503432), Julie Millet (127730), Christopher Brown (258061), Nalin Rastogi (674), Pierre Couppié (342022), David Couvin (130640), Eric Legrand (248989)   +6 more
core   +1 more source

Molecular typing of Mycobacterium kansasii using pulsed-field gel electrophoresis and a newly designed variable-number tandem repeat analysis

Scientific Reports, 2018
Molecular epidemiological studies of Mycobacterium kansasii are hampered by the lack of highly-discriminatory genotyping modalities. The purpose of this study was to design a new, high-resolution fingerprinting method for M. kansasii.
Zofia Bakuła, Anna Brzostek, Paulina Borówka, Anna Żaczek, Izabela Szulc-Kiełbik, Agata Podpora, Paweł Parniewski, Dominik Strapagiel, Jarosław Dziadek, Małgorzata Proboszcz, Jacek Bielecki, Jakko van Ingen, Tomasz Jagielski   +12 more
doaj   +1 more source

MDR-TB SIT41_MIRU-VNTR genotyping dataset

, 2017
<p>The table represents spoligo- and 24 loci MIRU-VNTR genotypes of MDR Mycobacterium tuberculosis strains from Bulgaria  </p ...
Stefan Panaiotov, Stefan Panaiotov (141413)   +1 more
core   +1 more source

Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR

Genome Medicine
Background Repetitive genome regions, such as variable number of tandem repeats (VNTR) or short tandem repeats (STR), are major constituents of the uncharted dark genome and evade conventional sequencing approaches. The protein-coding LPA kringle IV type-
Stephan Amstler, Gertraud Streiter, Cathrin Pfurtscheller, Lukas Forer, Silvia Di Maio, Hansi Weissensteiner, Bernhard Paulweber, Sebastian Schönherr, Florian Kronenberg, Stefan Coassin   +9 more
doaj   +1 more source

Origins and evolution of VNTR loci: The apolipoprotein B 3\u27 VNTR

, 1993
I studied the apolipoprotein (apo) B 3$\sp\prime$ variable number tandem repeat (VNTR) and did computer simulations of the stepwise mutation model to address four questions: (1) How did the apo B VNTR originate?
Shriver, Mark David
core   +1 more source