نتایج جستجو برای: resequencing

تعداد نتایج: 2156  

Journal: :Bioinformatics 2005
Yiping Zhan David Kulp

MOTIVATION Basecalling is a critical step of the analysis of DNA resequencing microarray data for single nucleotide polymorphism discovery and genotyping. For microarrays hybridized with DNA derived from diploid organisms, basecalling with high accuracy at high call rates is a challenging task. Current methods sometimes do not produce satisfactory results. RESULTS We explored using physical m...

2016
Feng Cheng Jian Wu Chengcheng Cai Lixia Fu Jianli Liang Theo Borm Mu Zhuang Yangyong Zhang Fenglan Zhang Guusje Bonnema Xiaowu Wang

The closely related species Brassica rapa and B. oleracea encompass a wide range of vegetable, fodder and oil crops. The release of their reference genomes has facilitated resequencing collections of B. rapa and B. oleracea aiming to build their variome datasets. These data can be used to investigate the evolutionary relationships between and within the different species and the domestication o...

2011
Michael E. Zwick Maureen Kiley Thomason Peter E. Chen Henry R. Johnson Shanmuga Sozhamannan Alfred Mateczun Timothy D. Read

We performed whole-genome amplification followed by hybridization of custom-designed resequencing arrays to resequence 303 kb of genomic sequence from a worldwide panel of 39 Bacillus anthracis strains. We used an efficient algorithm contained within a custom software program, UniqueMER, to identify and mask repetitive sequences on the resequencing array to reduce false-positive identification ...

Journal: :Genome research 2003
Raymond D Miller Shenghui Duan Elizabeth G Lovins Ellen F Kloss Pui-Yan Kwok

Targeted resequencing of genomic DNA from organisms such as humans is an important tool enabling experimental access to variation within the species and between similar species. Taking full advantage of the reference genome sequences in designing robust, specific PCR assays and using stringent conditions, resequencing can be done efficiently without purification of the PCR product. By using a 1...

Journal: :American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005
D L Grady A Harxhi M Smith P Flodman M A Spence J M Swanson R K Moyzis

A high prevalence of rare dopamine receptor D4 (DRD4) alleles in children diagnosed with attention-deficit hyperactivity disorder (ADHD) has been reported [Grady et al., 2003]. In this prior study, extensive resequencing/haplotype data of the DRD4 locus was used to suggest that population stratification was not the explanation for the high prevalence of rare alleles. In the current study, DNA r...

2016
Ambika Sahoo Basudeba Kar Suprava Sahoo Asit Ray Sanghamitra Nayak

Turmeric is an economically valued crop, because of its utility in the food, pharmaceutical industries and Ayurvedic medicine, attracts the attention in many areas of research work. In the present study, we executed resequencing through transcriptome assembly of the turmeric cultivar Suvarna (CL_Suv_10). Resequencing of Suvarna variety has generated 5 Gbases raw data with 75 bp paired-end seque...

Journal: :Blood 2008
Zhifu Xiang Yu Zhao Vesselin Mitaksov Daved H Fremont Yumi Kasai AnnaLynn Molitoris Rhonda E Ries Tracie L Miner Michael D McLellan John F DiPersio Daniel C Link Jacqueline E Payton Timothy A Graubert Mark Watson William Shannon Sharon E Heath Rakesh Nagarajan Elaine R Mardis Richard K Wilson Timothy J Ley Michael H Tomasson

Somatic mutations in JAK2 are frequently found in myeloproliferative diseases, and gain-of-function JAK3 alleles have been identified in M7 acute myeloid leukemia (AML), but a role for JAK1 in AML has not been described. We screened the entire coding region of JAK1 by total exonic resequencing of bone marrow DNA samples from 94 patients with de novo AML. We identified 2 novel somatic mutations ...

2011
Mohamad Saad Aude Saint Pierre Nora Bohossian Matthias Macé Maria Martinez

Genome-wide association studies for complex traits are based on the common disease/common variant (CDCV) and common disease/rare variant (CDRV) assumptions. Under the CDCV hypothesis, classical genome-wide association studies using single-marker tests are powerful in detecting common susceptibility variants, but under the CDRV hypothesis they are not as powerful. Several methods have been recen...

2006

I. THE SETUP At time t, let V (t) be the event {the DN is empty at time t}. If V̄ (t), let C∗(t) be the oldest customer in the DN, let W∗(t) be the time C∗(t) has spent in the DN, and let I∗(t) be the queue in the DN which C∗(t) goes through. For n ≥ 0, let E(t, s, n) = {at least n customers arrived at the DN on the interval (t− s, t], out of which at least n have left the DN by t}. Let the size...

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