Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Severe acute respiratory syndrome coronavirus 2 strain:NR-52282 | isolate:Hong Kong/VM20001061/2020

ABSTRACT: Severe acute respiratory syndrome coronavirus 2 strain:NR-52282 | isolate:Hong Kong/VM20001061/2020 Genome sequencing

PROVIDER: PRJNA636301 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Similar Datasets

Severe acute respiratory syndrome coronavirus 2 strain:Hong Kong/VM20001061/2020

Project description:Severe acute respiratory syndrome coronavirus 2 strain:Hong Kong/VM20001061/2020 Genome sequencing

| PRJNA639827 | ENA

Drosophila elegans strain:Hong Kong

Project description:Drosophila elegans strain:Hong Kong Genome sequencing and assembly

| PRJNA590036 | ENA

Hong Kong T2D-GENES Exome Sequencing Study

Project description:Hong Kong T2D-GENES Exome Sequencing Study

| PRJNA422325 | ENA

Hong Kong T2D-GENES Exome Sequencing Study

Project description:Hong Kong T2D-GENES Exome Sequencing Study

| PRJNA422326 | ENA

Environmental bacteria from Hong Kong seawater

Project description:Environmental bacteria from Hong Kong seawater Raw sequence reads

| PRJNA817672 | ENA

Citrus hindsii cultivar:Hong Kong kumquat

Project description:Citrus hindsii cultivar:Hong Kong kumquat Transcriptome or Gene expression

| PRJNA497956 | ENA

Hong Kong coastal waters

Project description:Raw sequence reads of rRNA of Chaetoceros, Pseudo-nitzschia, and Thalassiosira in Hong Kong coastal waters

| PRJNA1138948 | ENA

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

Project description:The project aim is to evaluate the role of whole-genome aCGH for prenatal diagnosis in Hong Kong. Array CGH was performed on 220 samples recruited prospectively as the first-tier test study; and on 150 samples with abnormal ultrasound findings and normal karyotypes as a further-test study using NimbleGen CGX-135K oligonucleotide arrays. After the exclusion of common aneuploidies in the first-tier study, clinically significant CNVs are detected in 23/220 samples. In the further test study, clinically significant CNVs are detected in 9/150 samples, which showed CGX array has an increased diagnostic yield of about 6% compared with conventional cytogenetic methods. CNVs of unclear clinical significance are detected in only 10/370 (2.7%) samples. Only data from sample with positive findings are included in this experiment submission (the samples with normal results are not included here).

2014-01-01 | E-MTAB-2156 | biostudies-arrayexpress

Characterization of Genomic Profile of Breast Tumors In Hong Kong

Project description:Characterization of Genomic Profile of Breast Tumors In Hong Kong

| PRJNA556915 | ENA

Characterization of Genomic Profile of Breast Tumors In Hong Kong

Project description:Characterization of Genomic Profile of Breast Tumors In Hong Kong

| PRJNA556914 | ENA