Transcriptome and epigenome analysis of engram cells: Next-generation sequencing technologies in memory research

by Alaiz-Noya, M., Barco, A., Fuentes-Ramos, M.
Published 2021

Extracting multi-way chromatin contacts from Hi-C data

by Hyeon, C., Liu, L., Zhang, B.
Published 2021

Analysis of five deep-sequenced trio-genomes of the Peninsular Malaysia Orang Asli and North Borneo populations

by Deng, L., Farhang, A., Hoh, B.-P, Hoque, M.Z, Jong, B., Kumar, S.V, Liu, C., Lou, H., Lu, D., Marshall, C.R, Ong, R.T.-H, Phipps, M.E, Scherer, S.W, Teo, Y.-Y, Thiruvahindrapuram, B., Thuhairah, A.R, Wong, L.-P, Xie, B., Xu, S., Xu, W., Yew, C.-W, Zhang, X.
Published 2019

Mitochondrial DNA mutations in Malaysian female breast cancer patients

by Abdullah, M.A, Ahmad, A.F, Ang, G.Y, Baghawi, A., Emran, N.A, Kitan, N., Maniam, S., Omasanggar, R., Teh, L.K, Yu, C.Y
Published 2020

Clinical and molecular genetic analysis of a Chinese family with hereditary elliptocytosis caused by a novel mutation in the EPB41 gene

by Cao, M., Huang, Z., Lin, J., Zhang, D., Zhou, H.
Published 2021

Rare case of intracranial hemorrhage associated with seoul virus infection diagnosed by metagenomic next-generation sequencing

by Bi, X., Huang, Z., Xian, Y., Xie, D., Xu, W., You, J., Yuan, X.
Published 2021

A comprehensive expression profile of tRNA-derived fragments in papillary thyroid cancer

by Shan, S., Wang, Y., Zhu, C.
Published 2021

A rare case of pulmonary nocardiosis comorbid with Sjogren’s syndrome

by Dong, X., Ge, Y., Lv, H., Peng, Y., Zhu, Y.
Published 2021

Identification of a novel heterozygous mutation in the MITF gene in an Iranian family with Waardenburg syndrome type II using next-generation sequencing

by Javanshir, N., Nasirshalal, M., Panahi, M., Salmani, H.
Published 2021

Detection of CYP2C19 genetic variants in Malaysian Orang Asli from massively parallel sequencing data

by Ahmad, A., Ang, G.Y, Aziz, T.A.T.A, Isa, K.M, Ismail, A.I, James, R.J, Khalid, M.I.H.A, Nor, F.M, Rahman, T.A, Salleh, H., Salleh, M.Z, Subramaniam, V., Teh, L.K, Yu, C.Y
Published 2016

Application of high-throughput sequencing for hereditary thrombocytopenia in southwestern China

by Dou, Y., Guan, X., Guo, Y., Luo, M., Wen, X., Xian, Y., Yu, J., Zhang, L.
Published 2021

Genome-based characterization of Escherichia coli causing bloodstream infection through next-generation sequencing

by Erlina, L., Fadilah, F., Nelwan, E.J, Paramita, R.I, Puspandari, N., Renesteen, E.
Published 2021

Multilocus sequence typing analysis and second-generation sequencing analysis of Salmonella Wandsworth

by Lu, Y., Wang, Y., Xu, X., Zhang, C.
Published 2021

Targeted resequencing showing novel common and rare genetic variants increases the risk of asthma in the Chinese Han population

by Cheng, Z., Deng, Y., Fang, S., Li, J., Li, Z., Liu, J., Luo, G., Luo, L., Mo, B., Shu, Y., Wang, Y., Wang, Z., Wei, J., Xiong, W., Yang, H., Yang, J., Yu, B., Zhang, X., Zhu, J.
Published 2021

A next generation sequencing-based protocol for screening of variants of concern in autism spectrum disorder

by Budjan, C., Fong, M., Huang, J., Jeong, M.-S, Kong, X.-J, Liu, J., Liu, K., Sherman, H.T, Tian, R., Zhuang, P.
Published 2022

Cross-platform comparison of next-generation sequencing and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry for detecting KRAS/NRAS/BRAF/PIK3CA mutatio...

by Cao, M., Chen, X., Guo, W., Huang, F., Jiang, H., Liu, T., Shen, M., Wang, B., Wang, H., Xu, X., Yang, Y., Yu, Y.
Published 2021

KMT2D promotes proliferation of gastric cancer cells: evidence from ctDNA sequencing

by Chen, Q., Li, Q., Wu, F., Wu, R.
Published 2021