Pesquisas alternativas:
chad como » chaid como (Expandir a Pesquisa), cad como (Expandir a Pesquisa), yihad como (Expandir a Pesquisa)
nail flap » snail flap (Expandir a Pesquisa), nail flag (Expandir a Pesquisa), tail flap (Expandir a Pesquisa)
flap case » flap based (Expandir a Pesquisa)
como can » como canal (Expandir a Pesquisa), como canon (Expandir a Pesquisa), como cande (Expandir a Pesquisa)
case non » cause non (Expandir a Pesquisa), case note (Expandir a Pesquisa), use non (Expandir a Pesquisa)
can ngos » can ngoc (Expandir a Pesquisa), can now (Expandir a Pesquisa)
can non » dan non (Expandir a Pesquisa), than non (Expandir a Pesquisa)
can ngs » can lungs (Expandir a Pesquisa), can ngoc (Expandir a Pesquisa), can nash (Expandir a Pesquisa)
m nail » m nabil (Expandir a Pesquisa), m nair (Expandir a Pesquisa), m nacl (Expandir a Pesquisa)
A mostrar 1 - 20 resultados de 55 para a pesquisa '(( j chad como can non ) OR ((( m nail flap case non ) OR ( j e tool ((can ngs) OR (can ngos)) ))))', tempo de pesquisa: 0.88seg Refinar resultados
Nimbus: a design-driven analyses suite for amplicon-based NGS data
Transcriptome analysis of the induction of somatic embryogenesis in Coffea canephora and the participation of ARF and Aux/IAA genes

RNA Deep Sequencing - Beyond Proof of Concept
exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels

GenePy - a score for estimating gene pathogenicity in individuals using next-generation sequencing data
A5 Near full-length HIV-1 genome sequencing in newly diagnosed individuals in Sweden

Sequencing Framework for the Sensitive Detection and Precise Mapping of Defective Interfering Particle-Associated Deletions across Influenza A and B Viruses
Next-generation sequencing identifies germline MRE11A variants as markers of radiotherapy outcomes in muscle-invasive bladder cancer

Novel Tools for Conservation Genomics: Comparing Two High-Throughput Approaches for SNP Discovery in the Transcriptome of the European Hake
Targeted resequencing of candidate genes using selector probes

Can community action improve equity for maternal health and how does it do so? Research findings from Gujarat, India
A ligation-based single-stranded library preparation method to analyze cell-free DNA and synthetic oligos

The use of chloroplast genome sequences to solve phylogenetic incongruences in Polystachya Hook (Orchidaceae Juss)
Adapterama II: universal amplicon sequencing on Illumina platforms (TaggiMatrix)

The Role of Next Generation Sequencing in Infection Prevention in Human Parainfluenza Virus 3 Infections in Immunocompromised Patients

A practical, bioinformatic workflow system for large data sets generated by next-generation sequencing
Towards the integration, annotation and association of historical microarray experiments with RNA-seq

Circulating tumor DNA quantity is related to tumor volume and both predict survival in metastatic pancreatic ductal adenocarcinoma
International Standards for Genomes, Transcriptomes, and Metagenomes

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