17 research outputs found

    Mapping and phasing of structural variation in patient genomes using nanopore sequencing

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    Despite improvements in genomics technology, the detection of structural variants (SVs) from short-read sequencing still poses challenges, particularly for complex variation. Here we analyse the genomes of two patients with congenital abnormalities using the MinION nanopore sequencer and a novel computational pipeline—NanoSV. We demonstrate that nanopore long reads are superior to short reads with regard to detection of de novo chromothripsis rearrangements. The long reads also enable efficient phasing of genetic variations, which we leveraged to determine the parental origin of all de novo chromothripsis breakpoints and to resolve the structure of these complex rearrangements. Additionally, genome-wide surveillance of inherited SVs reveals novel variants, missed in short-read data sets, a large proportion of which are retrotransposon insertions. We provide a first exploration of patient genome sequencing with a nanopore sequencer and demonstrate the value of long-read sequencing in mapping and phasing of SVs for both clinical and research applications

    Análise da Arborização de Quatro Praças no Bairro da Tijuca, RJ, Brasil

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    Neste estudo foi realizada a avaliação da arborização de quatro praças da Tijuca, Rio de Janeiro, RJ, considerando a riqueza de espécies, análises morfométricas dos indivíduos, além do seu diagnóstico fitossanitário. Foram encontradas 310 árvores, distribuídas em 36 espécies e 14 famílias, com destaque para Cassia siamea e Delonix regia que, juntas, corresponderam a 32,4% dos indivíduos. Cassia siamea representou 9,4% dos indivíduos da Praça Castilho França, 32,3% da Varnhagen, 24,0% da Saens Pena e 11,1% da Xavier de Brito. Já Delonix regia totalizou 3,2% das espécies da Praça Varnhagen, 10,7% da Saens Pena e 35,2% da Xavier de Brito. Nas quatro praças foi encontrada uma distribuição proporcional entre as espécies exóticas e nativas. Todavia, comparando o número de indivíduos, foi constatado predomínio das exóticas. Considerando todos os indivíduos amostrados, 83,6% concentraram-se entre 5 m e 15 m de altura. Observou-se que 49,5% das árvores apresentaram DAP maiores que 30 cm. Considerando-se os aspectos fitossanitários, 64,5% das árvores encontravam-se saudáveis e 25,4% mostravam sinais de ataques de pragas, além disso, 10,1% sofreram injúrias. Diante desses fatos, recomenda-se a substituição dos indivíduos debilitados que sejam uma ameaça aos usuários ou prejudiquem a estética, procurando sempre utilizar o maior número de espécies nativas possível, para evitar a uniformidade. Também se faz necessário intensificar o controle das pragas e as atividades de educação ambiental, com o intuito de reduzir os danos nos exemplares da flora das praças urbanas

    20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition

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    Intellectual disability (ID) is characterized by an extraordinary genetic heterogeneity, with >250 genes that have been implicated in monogenic forms of ID. Because this complexity precluded systematic testing for mutations and because clinical features are often non-specific, for some of these genes only few cases or families have been unambiguously documented. It is the case of the X-linked gene encoding monoamine oxidase A (MAOA), for which only one nonsense mutation has been identified in Brunner syndrome, characterized in a single family by mild non-dysmorphic ID and impulsive, violent and aggressive behaviors. We have performed targeted high-throughput sequencing of 220 genes, including MAOA, in patients with undiagnosed ID. We identified a c.797_798delinsTT (p.C266F) missense mutation in MAOA in a boy with autism spectrum disorder, attention deficit and autoaggressive behavior. Two maternal uncles carry the mutation and have severe ID, with a history of maltreatment in early childhood. This novel missense mutation decreases MAOA enzymatic activity, leading to abnormal levels of urinary monoamines. The identification of this new point mutation confirms, for the first time since 1993, the monogenic implication of the MAOA gene in ID of various degrees, autism and behavioral disturbances. The variable expressivity of the mutation observed in male patients of this family may involve gene–environment interactions, and the identification of a perturbation in monoamine metabolism should be taken into account when prescribing psychoactive drugs in such patients
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