Pesquisas alternativas:
nayl » nayla (Expandir a Pesquisa), natl (Expandir a Pesquisa), nail (Expandir a Pesquisa)
nowe » now (Expandir a Pesquisa), none (Expandir a Pesquisa), node (Expandir a Pesquisa)
gray » gram (Expandir a Pesquisa), gran (Expandir a Pesquisa)
carl » care (Expandir a Pesquisa), cal (Expandir a Pesquisa), call (Expandir a Pesquisa)
ngoc » ngo (Expandir a Pesquisa)
A mostrar 1 - 15 resultados de 15 para a pesquisa '(( j small compared can ngs ) OR ((( j nayl clamp j nowe ) OR ( j gray carl can ngoc ))))', tempo de pesquisa: 0.60seg Refinar resultados
Exploration of small RNA-seq data for small non-coding RNAs in Human Colorectal Cancer
Exosomes provide a protective and enriched source of miRNA for biomarker profiling compared to intracellular and cell-free blood

Quality Control and Pre-Qualification of NGS Libraries Made from Clinical Samples
Comparison of Clinical Targeted Next-Generation Sequence Data from Formalin-Fixed and Fresh-Frozen Tissue Specimens

Genomic Treasure Troves: Complete Genome Sequencing of Herbarium and Insect Museum Specimens
WISECONDOR: detection of fetal aberrations from shallow sequencing maternal plasma based on a within-sample comparison scheme

KRAS Mutation Detection in Non-small Cell Lung Cancer Using a Peptide Nucleic Acid-Mediated Polymerase Chain Reaction Clamping Method and Comparative Validation with Next-Generation Sequencing
Experience with targeted next generation sequencing for the care of lung cancer: insights into promises and limitations of genomic oncology in day-to-day practice

The correlation between crizotinib efficacy and molecular heterogeneity by next-generation sequencing in non-small cell lung cancer
5′/ 3′ imbalance strategy to detect ALK fusion genes in circulating tumor RNA from patients with non-small cell lung cancer

Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial Pseudarthrosis
Classification and Biomarker Genes Selection for Cancer Gene Expression Data Using Random Forest

Next generation sequencing-based molecular profiling of lung adenocarcinoma using pleural effusion specimens
Reconstructing Breakage Fusion Bridge Architectures Using Noisy Copy Numbers

Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform
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