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1.
DNA Res ; 26(4): 313-325, 2019 Aug 01.
Article in English | MEDLINE | ID: mdl-31173071

ABSTRACT

The diversity of disease presentations warrants one single assay for detection and delineation of various genomic disorders. Herein, we describe a gel-free and biotin-capture-free mate-pair method through coupling Controlled Polymerizations by Adapter-Ligation (CP-AL). We first demonstrated the feasibility and ease-of-use in monitoring DNA nick translation and primer extension by limiting the nucleotide input. By coupling these two controlled polymerizations by a reported non-conventional adapter-ligation reaction 3' branch ligation, we evidenced that CP-AL significantly increased DNA circularization efficiency (by 4-fold) and was applicable for different sequencing methods but at a faction of current cost. Its advantages were further demonstrated by fully elimination of small-insert-contaminated (by 39.3-fold) with a ∼50% increment of physical coverage, and producing uniform genome/exome coverage and the lowest chimeric rate. It achieved single-nucleotide variants detection with sensitivity and specificity up to 97.3 and 99.7%, respectively, compared with data from small-insert libraries. In addition, this method can provide a comprehensive delineation of structural rearrangements, evidenced by a potential diagnosis in a patient with oligo-atheno-terato-spermia. Moreover, it enables accurate mutation identification by integration of genomic variants from different aberration types. Overall, it provides a potential single-integrated solution for detecting various genomic variants, facilitating a genetic diagnosis in human diseases.


Subject(s)
Genome-Wide Association Study/methods , Genotyping Techniques/methods , Polymorphism, Single Nucleotide , Sequence Analysis, DNA/methods , Genetic Predisposition to Disease , Humans , Infertility, Male/genetics , Male
2.
Genome Res ; 25(3): 426-34, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25672852

ABSTRACT

Currently, the methods available for preimplantation genetic diagnosis (PGD) of in vitro fertilized (IVF) embryos do not detect de novo single-nucleotide and short indel mutations, which have been shown to cause a large fraction of genetic diseases. Detection of all these types of mutations requires whole-genome sequencing (WGS). In this study, advanced massively parallel WGS was performed on three 5- to 10-cell biopsies from two blastocyst-stage embryos. Both parents and paternal grandparents were also analyzed to allow for accurate measurements of false-positive and false-negative error rates. Overall, >95% of each genome was called. In the embryos, experimentally derived haplotypes and barcoded read data were used to detect and phase up to 82% of de novo single base mutations with a false-positive rate of about one error per Gb, resulting in fewer than 10 such errors per embryo. This represents a ∼ 100-fold lower error rate than previously published from 10 cells, and it is the first demonstration that advanced WGS can be used to accurately identify these de novo mutations in spite of the thousands of false-positive errors introduced by the extensive DNA amplification required for deep sequencing. Using haplotype information, we also demonstrate how small de novo deletions could be detected. These results suggest that phased WGS using barcoded DNA could be used in the future as part of the PGD process to maximize comprehensiveness in detecting disease-causing mutations and to reduce the incidence of genetic diseases.


Subject(s)
Embryo, Mammalian , Fertilization in Vitro , Genome, Human , High-Throughput Nucleotide Sequencing , Point Mutation , Blastocyst/metabolism , Exons , Haplotypes , Heterozygote , Humans , Polymorphism, Single Nucleotide , Sequence Deletion
3.
Nature ; 487(7406): 190-5, 2012 Jul 11.
Article in English | MEDLINE | ID: mdl-22785314

ABSTRACT

Recent advances in whole-genome sequencing have brought the vision of personal genomics and genomic medicine closer to reality. However, current methods lack clinical accuracy and the ability to describe the context (haplotypes) in which genome variants co-occur in a cost-effective manner. Here we describe a low-cost DNA sequencing and haplotyping process, long fragment read (LFR) technology, which is similar to sequencing long single DNA molecules without cloning or separation of metaphase chromosomes. In this study, ten LFR libraries were made using only ∼100 picograms of human DNA per sample. Up to 97% of the heterozygous single nucleotide variants were assembled into long haplotype contigs. Removal of false positive single nucleotide variants not phased by multiple LFR haplotypes resulted in a final genome error rate of 1 in 10 megabases. Cost-effective and accurate genome sequencing and haplotyping from 10-20 human cells, as demonstrated here, will enable comprehensive genetic studies and diverse clinical applications.


Subject(s)
Genome, Human , Genomics/methods , Sequence Analysis, DNA/methods , Alleles , Cell Line , Female , Gene Silencing , Genetic Variation , Haplotypes , Humans , Mutation , Reproducibility of Results , Sequence Analysis, DNA/economics , Sequence Analysis, DNA/standards
4.
Chem Biol Interact ; 171(2): 212-35, 2008 Jan 30.
Article in English | MEDLINE | ID: mdl-17950718

ABSTRACT

Analysis of 16S rRNA sequences is a commonly used method for the identification and discrimination of microorganisms. However, the high similarity of 16S and 23S rRNA sequences of Bacillus cereus group organisms (up to 99-100%) and repeatedly failed attempts to develop molecular typing systems that would use DNA sequences to discriminate between species within this group have resulted in several suggestions to consider B. cereus and B. thuringiensis, or these two species together with B. anthracis, as one species. Recently, we divided the B. cereus group into seven subgroups, Anthracis, Cereus A and B, Thuringiensis A and B, and Mycoides A and B, based on 16S rRNA, 23S rRNA and gyrB gene sequences and identified subgroup-specific makers in each of these three genes. Here we for the first time demonstrated discrimination of these seven subgroups, including subgroup Anthracis, with a 3D gel element microarray of oligonucleotide probes targeting 16S and 23S rRNA markers. This is the first microarray enabled identification of B. anthracis and discrimination of these seven subgroups in pure cell cultures and in environmental samples using rRNA sequences. The microarray bearing perfect match/mismatch (p/mm) probe pairs was specific enough to discriminate single nucleotide polymorphisms (SNPs) and was able to identify targeted organisms in 5min. We also demonstrated the ability of the microarray to determine subgroup affiliations for B. cereus group isolates without rRNA sequencing. Correlation of these seven subgroups with groupings based on multilocus sequence typing (MLST), fluorescent amplified fragment length polymorphism analysis (AFLP) and multilocus enzyme electrophoresis (MME) analysis of a wide spectrum of different genes, and the demonstration of subgroup-specific differences in toxin profiles, psychrotolerance, and the ability to harbor some plasmids, suggest that these seven subgroups are not based solely on neutral genomic polymorphisms, but instead reflect differences in both the genotypes and phenotypes of the B. cereus group organisms.


Subject(s)
Bacillus anthracis/isolation & purification , RNA, Ribosomal, 16S/analysis , RNA, Ribosomal, 23S/analysis , Bacillus anthracis/genetics , Base Sequence , Molecular Sequence Data , Oligonucleotide Array Sequence Analysis , Polymorphism, Single Nucleotide , RNA, Ribosomal, 16S/genetics , RNA, Ribosomal, 23S/genetics , Sequence Homology, Nucleic Acid , Species Specificity
5.
J Clin Microbiol ; 44(1): 244-50, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16390982

ABSTRACT

A genome-independent microarray and new statistical techniques were used to genotype Bacillus strains and quantitatively compare DNA fingerprints with the known taxonomy of the genus. A synthetic DNA standard was used to understand process level variability and lead to recommended standard operating procedures for microbial forensics and clinical diagnostics.


Subject(s)
Bacillus/isolation & purification , Bacterial Typing Techniques , Oligonucleotide Array Sequence Analysis/methods , Bacillus/classification , Bacillus/genetics , DNA Fingerprinting/methods , Genome, Bacterial , Nucleic Acid Hybridization , Phylogeny
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