Evidence map›Paper›PMID 29474353›Full record

ArticlePLoS genetics2018

Deep sequencing of HBV pre-S region reveals high heterogeneity of HBV genotypes and associations of word pattern frequencies with HCC.

Xin Bai, Jian-An Jia, Meng Fang, Shipeng Chen, Xiaotao Liang, Shanfeng Zhu, Shuqin Zhang, Jianfeng Feng, Fengzhu Sun, Chunfang Gao

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Xin BaiCentre for Computational Systems Biology, School of Mathematical Sciences, Fudan University, Shanghai, China.ORCID 0000-0002-3755-0730
Jian-An JiaDepartment of Laboratory Medicine, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Meng FangDepartment of Laboratory Medicine, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Shipeng ChenDepartment of Laboratory Medicine, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Xiaotao LiangInstitute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, China.
Shanfeng ZhuSchool of Computer Science and Shanghai Key Lab of Intelligent Information Processing, Fudan University, Shanghai, China.
Shuqin ZhangCentre for Computational Systems Biology, School of Mathematical Sciences, Fudan University, Shanghai, China.
Jianfeng FengCentre for Computational Systems Biology, School of Mathematical Sciences, Fudan University, Shanghai, China.
Fengzhu SunCentre for Computational Systems Biology, School of Mathematical Sciences, Fudan University, Shanghai, China.ORCID 0000-0002-8552-043X
Chunfang GaoDepartment of Laboratory Medicine, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Fudan University · CNSecond Military Medical University · CNUniversity of Southern California · US

Funding

Computational Studies of Virus-host Interactions Using Metagenomics Data and ApplicationsR01GM120624 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI AHLGREN, NATHAN, SUN, FENGZHU · 2017 to 2020
$1.7M
NIGMS NIH HHS R01 GM120624NIH HHS R01GM120624
6 · The paper itself

Abstract

Hepatitis B virus (HBV) infection is a common problem in the world, especially in China. More than 60-80% of hepatocellular carcinoma (HCC) cases can be attributed to HBV infection in high HBV prevalent regions. Although traditional Sanger sequencing has been extensively used to investigate HBV sequences, NGS is becoming more commonly used. Further, it is unknown whether word pattern frequencies of HBV reads by Next Generation Sequencing (NGS) can be used to investigate HBV genotypes and predict HCC status. In this study, we used NGS to sequence the pre-S region of the HBV sequence of 94 HCC patients and 45 chronic HBV (CHB) infected individuals. Word pattern frequencies among the sequence data of all individuals were calculated and compared using the Manhattan distance. The individuals were grouped using principal coordinate analysis (PCoA) and hierarchical clustering. Word pattern frequencies were also used to build prediction models for HCC status using both K-nearest neighbors (KNN) and support vector machine (SVM). We showed the extremely high power of analyzing HBV sequences using word patterns. Our key findings include that the first principal coordinate of the PCoA analysis was highly associated with the fraction of genotype B (or C) sequences and the second principal coordinate was significantly associated with the probability of having HCC. Hierarchical clustering first groups the individuals according to their major genotypes followed by their HCC status. Using cross-validation, high area under the receiver operational characteristic curve (AUC) of around 0.88 for KNN and 0.92 for SVM were obtained. In the independent data set of 46 HCC patients and 31 CHB individuals, a good AUC score of 0.77 was obtained using SVM. It was further shown that 3000 reads for each individual can yield stable prediction results for SVM. Thus, another key finding is that word patterns can be used to predict HCC status with high accuracy. Therefore, our study shows clearly that word pattern frequencies of HBV sequences contain much information about the composition of different HBV genotypes and the HCC status of an individual.

Indexed as

Genetic HeterogeneityCarcinoma, HepatocellularDNA FingerprintingDNA, ViralGene FrequencyGenetic Association StudiesGenotypeHepatitis B, ChronicHepatitis B Surface AntigensHepatitis B virusHigh-Throughput Nucleotide SequencingHumansLiver NeoplasmsPhylogenyProtein PrecursorsDNA, ViralHepatitis B Surface Antigenspresurface protein 1, hepatitis B surface antigenpresurface protein 2, hepatitis B surface antigenProtein Precursors

Identifiers

PMID29474353
PMCPMC5841821
OpenAlexW2787972083

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.