Cargando…

EASER: Ensembl Easy Sequence Retriever

The rapid advances in genome sequencing technologies have increased the pace at which biological sequence databases are becoming available to the broad scientific community. Thus, obtaining and preparing an appropriate sequence dataset is a crucial first step for all types of genomic analyses. Here,...

Descripción completa

Detalles Bibliográficos
Autores principales:	Maldonado, Emanuel, Khan, Imran, Philip, Siby, Vasconcelos, Vítor, Antunes, Agostinho
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Libertas Academica 2013
Materias:	Technical Advance
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855309/ https://www.ncbi.nlm.nih.gov/pubmed/24324324 http://dx.doi.org/10.4137/EBO.S11335

Ejemplares similares

An easy operating pathogen microarray (EOPM) platform for rapid screening of vertebrate pathogens
por: Huang, Weiwei, et al.
Publicado: (2013)

Good exams made easy: The item management system for multiple examination formats
por: Hochlehnert, Achim, et al.
Publicado: (2012)

VarCon: An R Package for Retrieving Neighboring Nucleotides of an SNV
por: Ptok, Johannes, et al.
Publicado: (2020)

Method for the location of primary wear scars from retrieved metal on metal hip replacements
por: Govind, Garima, et al.
Publicado: (2015)

Gait characterization in golden retriever muscular dystrophy dogs using linear discriminant analysis
por: Fraysse, Bodvaël, et al.
Publicado: (2017)

Exploring the Adenylation Domain Repertoire of Nonribosomal Peptide Synthetases Using an Ensemble of Sequence-Search Methods
por: Agüero-Chapin, Guillermin, et al.
Publicado: (2013)

Tissue Harvester with Functional Valve (THFV): Shidham's device for reproducibly higher specimen yield by fine needle aspiration biopsy with easy to perform steps
por: Shidham, Vinod B, et al.
Publicado: (2007)

paraFaceTest: an ensemble of regression tree-based facial features extraction for efficient facial paralysis classification
por: Barbosa, Jocelyn, et al.
Publicado: (2019)

High-recovery visual identification and single-cell retrieval of circulating tumor cells for genomic analysis using a dual-technology platform integrated with automated immunofluorescence staining
por: Campton, Daniel E, et al.
Publicado: (2015)

LMAP: Lightweight Multigene Analyses in PAML
por: Maldonado, Emanuel, et al.
Publicado: (2016)

Mapping‐by‐sequencing in complex polyploid genomes using genic sequence capture: a case study to map yellow rust resistance in hexaploid wheat
por: Gardiner, Laura‐Jayne, et al.
Publicado: (2016)

Analytical performance evaluation of a commercial next generation sequencing liquid biopsy platform using plasma ctDNA, reference standards, and synthetic serial dilution samples derived from normal plasma
por: Verma, Suman, et al.
Publicado: (2020)

Anchoring and ordering NGS contig assemblies by population sequencing (POPSEQ)
por: Mascher, Martin, et al.
Publicado: (2013)

Targeted next generation sequencing as a tool for precision medicine
por: Gulilat, Markus, et al.
Publicado: (2019)

Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
por: Khan, Imran, et al.
Publicado: (2014)

A sequence-anchored genetic linkage map for the moss, Physcomitrella patens
por: Kamisugi, Yasuko, et al.
Publicado: (2008)

A simple method for gene phasing using mate pair sequencing
por: Cradic, Kendall W, et al.
Publicado: (2014)

An improved sequencing-based strategy to estimate locus-specific DNA methylation
por: Brisotto, Giulia, et al.
Publicado: (2015)

An innovative method for manufacturing the Tuebingen palatal plate for infants with Robin sequence
por: Müller-Hagedorn, Silvia, et al.
Publicado: (2020)

Resistance gene enrichment sequencing (RenSeq) enables reannotation of the NB-LRR gene family from sequenced plant genomes and rapid mapping of resistance loci in segregating populations
por: Jupe, Florian, et al.
Publicado: (2013)

Rapid multiplex MinION nanopore sequencing workflow for Influenza A viruses
por: King, Jacqueline, et al.
Publicado: (2020)

The Wuerzburg procedure: the tensor fasciae latae perforator is a reliable anatomical landmark to clearly identify the Hueter interval when using the minimally-invasive direct anterior approach to the hip joint
por: Rudert, Maximilian, et al.
Publicado: (2016)

Adaptation of the Mitochondrial Genome in Cephalopods: Enhancing Proton Translocation Channels and the Subunit Interactions
por: Almeida, Daniela, et al.
Publicado: (2015)

AGUIA: autonomous graphical user interface assembly for clinical trials semantic data services
por: Correa, Miria C, et al.
Publicado: (2010)

Genome-wide capture sequencing to detect hepatitis C virus at the end of antiviral therapy
por: Peng, Peng, et al.
Publicado: (2020)

Detection of methylation in promoter sequences by melting curve analysis-based semiquantitative real time PCR
por: Lorente, Aiala, et al.
Publicado: (2008)

Fine needle aspirates of kidneys: a promising tool for RNA sequencing in native and transplanted kidneys
por: Eikrem, Øystein, et al.
Publicado: (2018)

Identification of single nucleotide variants using position-specific error estimation in deep sequencing data
por: Kleftogiannis, Dimitrios, et al.
Publicado: (2019)

DNA sequencing of anatomy lab cadavers to provide hands-on precision medicine introduction to medical students
por: Anandakrishnan, Ramu, et al.
Publicado: (2020)

Antimalarial antibody repertoire defined by plasma IG proteomics and single B cell IG sequencing
por: Coelho, Camila H., et al.
Publicado: (2020)

Sequence diversity within the HA-1 gene as detected by melting temperature assay without oligonucleotide probes
por: Graziano, Claudio, et al.
Publicado: (2005)

High resolution melting analysis for a rapid identification of heterozygous and homozygous sequence changes in the MUTYH gene
por: Tricarico, Rossella, et al.
Publicado: (2011)

Comprehensive assessment of knee joint synovitis at 7 T MRI using contrast-enhanced and non-enhanced sequences
por: Treutlein, Christoph, et al.
Publicado: (2020)

De novo chromosome level assembly of a plant genome from long read sequence data
por: Sharma, Priyanka, et al.
Publicado: (2021)

Biomarker discovery: quantification of microRNAs and other small non-coding RNAs using next generation sequencing
por: Lopez, Juan Pablo, et al.
Publicado: (2015)

Comparative evaluation of the new FDA approved THxID™-BRAF test with high resolution melting and sanger sequencing
por: Marchant, Julie, et al.
Publicado: (2014)

Comparison of Sanger sequencing for hepatitis C virus genotyping with a commercial line probe assay in a tertiary hospital
por: Goletti, Sylvie, et al.
Publicado: (2019)

Haplotyping by linked-read sequencing (HLRS) of the genetic disease carriers for preimplantation genetic testing without a proband or relatives
por: Li, Qing, et al.
Publicado: (2020)

Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis
por: Winkel, Bo G, et al.
Publicado: (2011)

Identification of Avramr1 from Phytophthora infestans using long read and cDNA pathogen‐enrichment sequencing (PenSeq)
por: Lin, Xiao, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_67si4soufgbfqounq71ms8c5a3