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**Overlapping of HPR0 and HPR7b variant sequence.
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创建时间：
2015-12-02
相关数据集
Additional file 7: Table S5. of Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis
Monoallelic rare variants with in silico pathogenic predictions identified in the 1000 Genomes cohort. (XLSX 100 kb)
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MOESM1 of Natural and pathogenic protein sequence variation affecting prion-like domains within and across human proteomes
Additional file 1. PAPA scores derived from random sampling of sequence variant combinations for proteins with high-scoring PrLDs. For all proteins with a moderately high-scoring PrLD (PAPA> 0.0) an
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Number of ribosomal sequence variants (RSVs) for each of the main symbiont genera characterized in the entire data set.
Number of ribosomal sequence variants (RSVs) for each of the main symbiont genera characterized in the entire data set.
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Detection and differentiation of Entamoeba histolytica and Entamoeba dispar in clinical samples through PCR-denaturing gradient gel electrophoresis
Amebiasis is one of the twenty major causes of disease in Mexico; however, the diagnosis is difficult due to limitations of conventional microscopy-based techniques. In this study, we analyzed stool s
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Next Generation Sequencing Studies on the HVR1 Region of Pakistani Isolates of Hepatitis C Virus
This project is aimed to evaluate the sequence variations of Hypervariable Region 1 (HVR1) of Hepatitis C virus isolates which were sampled from non-high risk HCV-infected population of Pakistan. Vari
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