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日志文件未找到 bibtex

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日志文件未找到 bibtex

当我尝试编译我的 bibtex 文件时，只有某些参考文献会出现并被编号。然而，许多其他参考文献却没有出现，而当我使用 bibtex 命令时，我收到“错误 - 未找到日志文件！”。我已对所有参考文献使用了 \cite{}，其中一些参考文献显示为问号，尽管它存在于 bib 文件中。

请查看我的 .bib 文件

@article{cargill1999characterization,
  title={Characterization of single-nucleotide polymorphisms in coding regions of human genes},
  author={Cargill, Michele and Altshuler, David and Ireland, James and Sklar, Pamela and Ardlie, Kristin and Patil, Nila and Lane, Charles R and Lim, Esther P and Kalyanaraman, Nilesh and Nemesh, James and others},
  journal={Nature genetics},
  volume={22},
  number={3},
  pages={231--238},
  year={1999},
  publisher={Nature Publishing Group}
}

@article{collins1998dna,
  title={A DNA polymorphism discovery resource for research on human genetic variation},
  author={Collins, Francis S and Brooks, Lisa D and Chakravarti, Aravinda},
  journal={Genome research},
  volume={8},
  number={12},
  pages={1229--1231},
  year={1998},
  publisher={Cold Spring Harbor Lab}
}

@article{frazer2009human,
  title={Human genetic variation and its contribution to complex traits},
  author={Frazer, Kelly A and Murray, Sarah S and Schork, Nicholas J and Topol, Eric J},
  journal={Nature Reviews Genetics},
  volume={10},
  number={4},
  pages={241--251},
  year={2009},
  publisher={Nature Publishing Group}
}

@article{10002010map,
  title={A map of human genome variation from population-scale sequencing},
  author={1000 Genomes Project Consortium and others},
  journal={Nature},
  volume={467},
  number={7319},
  pages={1061--1073},
  year={2010},
  publisher={Nature Publishing Group}
}

@article{smigielski2000dbsnp,
  title={dbSNP: a database of single nucleotide polymorphisms},
  author={Smigielski, Elizabeth M and Sirotkin, Karl and Ward, Minghong and Sherry, Stephen T},
  journal={Nucleic Acids Research},
  volume={28},
  number={1},
  pages={352--355},
  year={2000},
  publisher={Oxford Univ Press}
}

@article{fredman2002hgvbase,
  title={HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources},
  author={Fredman, D and Siegfried, Marianne and Yuan, Yan P. and Bork, Peer and Lehv{\"a}slaiho, Heikki and Brookes, Anthony J},
  journal={Nucleic acids research},
  volume={30},
  number={1},
  pages={387--391},
  year={2002},
  publisher={Oxford Univ Press}
}

@article{hamosh2005online,
  title={Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders},
  author={Hamosh, Ada and Scott, Alan F and Amberger, Joanna S and Bocchini, Carol A and McKusick, Victor A},
  journal={Nucleic acids research},
  volume={33},
  number={suppl 1},
  pages={D514--D517},
  year={2005},
  publisher={Oxford Univ Press}
}

@article{becker2004genetic,
  title={The genetic association database},
  author={Becker, Kevin G and Barnes, Kathleen C and Bright, Tiffani J and Wang, S Alex},
  journal={Nature genetics},
  volume={36},
  number={5},
  pages={431--432},
  year={2004},
  publisher={Nature Publishing Group}
}

@article{cooper1998human,
  title={The human gene mutation database},
  author={Cooper, David N and Ball, Edward V and Krawczak, Michael},
  journal={Nucleic acids research},
  volume={26},
  number={1},
  pages={285--287},
  year={1998},
  publisher={Oxford Univ Press}
}

@article{karolchik2003ucsc,
  title={The UCSC genome browser database},
  author={Karolchik, Donna and Baertsch, Robert and Diekhans, Mark and Furey, Terrence S. and Hinrichs, A and Lu, YT and Roskin, Krishna M. and Schwartz, M and Sugnet, Charles W. and Thomas, Daryl J and others},
  journal={Nucleic acids research},
  volume={31},
  number={1},
  pages={51--54},
  year={2003},
  publisher={Oxford Univ Press}
}

@article{adzhubei2010method,
  title={A method and server for predicting damaging missense mutations},
  author={Adzhubei, Ivan A and Schmidt, Steffen and Peshkin, Leonid and Ramensky, Vasily E and Gerasimova, Anna and Bork, Peer and Kondrashov, Alexey S and Sunyaev, Shamil R},
  journal={Nature methods},
  volume={7},
  number={4},
  pages={248--249},
  year={2010},
  publisher={Nature Publishing Group}
}

@article{ng2003sift,
  title={SIFT: Predicting amino acid changes that affect protein function},
  author={Ng, Pauline C and Henikoff, Steven},
  journal={Nucleic acids research},
  volume={31},
  number={13},
  pages={3812--3814},
  year={2003},
  publisher={Oxford Univ Press}
}

@article{kumar2012evolutionary,
  title={Evolutionary diagnosis method for variants in personal exomes},
  author={Kumar, Sudhir and Sanderford, Maxwell and Gray, Vanessa E and Ye, Jieping and Liu, Li},
  journal={Nature methods},
  volume={9},
  number={9},
  pages={855--856},
  year={2012},
  publisher={Nature Publishing Group}
}

@article{hicks2011prediction,
  title={Prediction of missense mutation functionality depends on both the algorithm and sequence alignment employed},
  author={Hicks, Stephanie and Wheeler, David A and Plon, Sharon E and Kimmel, Marek},
  journal={Human mutation},
  volume={32},
  number={6},
  pages={661--668},
  year={2011},
  publisher={Wiley Online Library}
}

@article{lopes2012combined,
  title={A combined functional annotation score for non-synonymous variants},
  author={Lopes, Margarida C and Joyce, Chris and Ritchie, Graham RS and John, Sally L and Cunningham, Fiona and Asimit, Jennifer and Zeggini, Eleftheria},
  journal={Human heredity},
  volume={73},
  number={1},
  pages={47--51},
  year={2012},
  publisher={Karger Publishers}
}

@article{capriotti2011improving,
  title={Improving the prediction of disease-related variants using protein three-dimensional structure},
  author={Capriotti, Emidio and Altman, Russ B},
  journal={BMC bioinformatics},
  volume={12},
  number={Suppl 4},
  pages={S3},
  year={2011},
  publisher={BioMed Central Ltd}
}

@article{bromberg2007snap,
  title={SNAP: predict effect of non-synonymous polymorphisms on function},
  author={Bromberg, Yana and Rost, Burkhard},
  journal={Nucleic acids research},
  volume={35},
  number={11},
  pages={3823--3835},
  year={2007},
  publisher={Oxford Univ Press}
}

@article{bromberg2007snap,
  title={SNAP: predict effect of non-synonymous polymorphisms on function},
  author={Bromberg, Yana and Rost, Burkhard},
  journal={Nucleic acids research},
  volume={35},
  number={11},
  pages={3823--3835},
  year={2007},
  publisher={Oxford Univ Press}
}

@article{collins2001implications,
  title={Implications of the Human Genome Project for medical science},
  author={Collins, Francis S and McKusick, Victor A},
  journal={Jama},
  volume={285},
  number={5},
  pages={540--544},
  year={2001},
  publisher={American Medical Association}
}

@article{lyons2009sail,
  title={The SAIL databank: linking multiple health and social care datasets},
  author={Lyons, Ronan A and Jones, Kerina H and John, Gareth and Brooks, Caroline J and Verplancke, Jean-Philippe and Ford, David V and Brown, Ginevra and Leake, Ken},
  journal={BMC Medical Informatics and Decision Making},
  volume={9},
  number={1},
  pages={3},
  year={2009},
  publisher={BioMed Central Ltd}
}

@article{guttmacher2002genomic,
  title={Genomic medicine—a primer},
  author={Guttmacher, Alan E and Collins, Francis S and Guttmacher, Alan E and Collins, Francis S},
  journal={New England Journal of Medicine},
  volume={347},
  number={19},
  pages={1512--1520},
  year={2002},
  publisher={Mass Medical Soc}
}

@article{green2011charting,
  title={Charting a course for genomic medicine from base pairs to bedside},
  author={Green, Eric D and Guyer, Mark S and Institute, National Human Genome Research and others},
  journal={Nature},
  volume={470},
  number={7333},
  pages={204--213},
  year={2011},
  publisher={Nature Publishing Group}
}

@article{ginsburg2001personalized,
  title={Personalized medicine: revolutionizing drug discovery and patient care},
  author={Ginsburg, Geoffrey S and McCarthy, Jeanette J},
  journal={TRENDS in Biotechnology},
  volume={19},
  number={12},
  pages={491--496},
  year={2001},
  publisher={Elsevier}
}

@article{kho2013practical,
  title={Practical challenges in integrating genomic data into the electronic health record},
  author={Kho, Abel N and Rasmussen, Luke V and Connolly, John J and Peissig, Peggy L and Starren, Justin and Hakonarson, Hakon and Hayes, M Geoffrey},
  journal={Genetics in Medicine},
  volume={15},
  number={10},
  pages={772--778},
  year={2013},
  publisher={Nature Publishing Group}
}

@article{martin2002lntegratingfienomics,
  title={lntegratingfienomics into Health Information Systems},
  author={Martin-Sanchez, F and Mooio, V and Lopez-CamposI, G},
  journal={Methods Inf Med},
  volume={4},
  pages={25--30},
  year={2002}
}

@article{decode,
  title={deCODE: A Genealogical Approach to Human Genetics in Iceland},
  author={Jeffrey R Gulcher, Kari Stefansson},
  year={2006},
  publisher={Wiley}
}

@article{roden2008development,
  title={Development of a large-scale de-identified DNA biobank to enable personalized medicine},
  author={Roden, Dan M and Pulley, Jill M and Basford, Melissa A and Bernard, Gordon R and Clayton, Ellen W and Balser, Jeffrey R and Masys, Dan R},
  journal={Clinical Pharmacology \& Therapeutics},
  volume={84},
  number={3},
  pages={362--369},
  year={2008},
  publisher={Nature Publishing Group}
}

@article{kullo2010genome,
  title={A genome-wide association study of red blood cell traits using the electronic medical record},
  author={Kullo, Iftikhar J and Ding, Keyue and Jouni, Hayan and Smith, Carin Y and Chute, Christopher G},
  journal={PLoS One},
  volume={5},
  number={9},
  pages={e13011},
  year={2010},
  publisher={Public Library of Science}
}

@article{siva20081000,
  title={1000 Genomes project},
  author={Siva, Nayanah},
  journal={Nature biotechnology},
  volume={26},
  number={3},
  pages={256--256},
  year={2008},
  publisher={Nature Publishing Group}
}

@article{gibbs2003international,
  title={The international HapMap project},
  author={Gibbs, Richard A and Belmont, John W and Hardenbol, Paul and Willis, Thomas D and Yu, Fuli and Yang, Huanming and Ch'ang, Lan-Yang and Huang, Wei and Liu, Bin and Shen, Yan and others},
  journal={Nature},
  volume={426},
  number={6968},
  pages={789--796},
  year={2003},
  publisher={Nature Publishing Group}
}

@article{mailman2007ncbi,
  title={The NCBI dbGaP database of genotypes and phenotypes},
  author={Mailman, Matthew D and Feolo, Michael and Jin, Yumi and Kimura, Masato and Tryka, Kimberly and Bagoutdinov, Rinat and Hao, Luning and Kiang, Anne and Paschall, Justin and Phan, Lon and others},
  journal={Nature genetics},
  volume={39},
  number={10},
  pages={1181--1186},
  year={2007},
  publisher={Nature Publishing Group}
}

@article{meigs2007genome,
  title={Genome-wide association with diabetes-related traits in the Framingham Heart Study},
  author={Meigs, James B and Manning, Alisa K and Fox, Caroline S and Florez, Jose C and Liu, Chunyu and Cupples, L Adrienne and Dupuis, Jos{\'e}e},
  journal={BMC medical genetics},
  volume={8},
  number={Suppl 1},
  pages={S16},
  year={2007},
  publisher={BioMed Central Ltd}
}

@article{wong2012prediction,
  title={Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors},
  author={Wong, ML and Dong, C and Andreev, V and Arcos-Burgos, M and Licinio, J},
  journal={Molecular psychiatry},
  volume={17},
  number={6},
  pages={624--633},
  year={2012},
  publisher={Nature Publishing Group}
}

@article{yucebacs2014prostate,
  title={A prostate cancer model build by a novel SVM-ID3 hybrid feature selection method using both genotyping and phenotype data from dbGaP},
  author={Y{\"u}ceba{\c{s}}, Sait Can and Son, Ye{\c{s}}im Ayd{\i}n},
  journal={PloS one},
  volume={9},
  number={3},
  pages={e91404},
  year={2014},
  publisher={Public Library of Science}
}

@article{cheadle1993direct,
  title={Direct sequencing of the complete CFTR gene: the molecular characterisation of 99.5\% of CF chromosomes in Wales},
  author={Cheadle, Jeremy P and Goodchild, Mary C and Meredith, Alison L},
  journal={Human molecular genetics},
  volume={2},
  number={10},
  pages={1551--1556},
  year={1993},
  publisher={Oxford Univ Press}
}

@article{lancaster1998brca1,
  title={BRCA1 and BRCA2 in breast cancer families from Wales: moderate mutation frequency and two recurrent mutations in BRCA1.},
  author={Lancaster, JM and Carney, ME and Gray, J and Myring, J and Gumbs, C and Sampson, J and Wheeler, D and France, E and Wiseman, R and Harper, P and others},
  journal={British journal of cancer},
  volume={78},
  number={11},
  pages={1417},
  year={1998},
  publisher={Nature Publishing Group}
}

@article{haralambos20121,
  title={(1) Genetic testing for familial hypercholesterolaemia in wales: identification of recurrent and novel variants},
  author={Haralambos, K and Whatley, S and Datta, D and McDowell, I},
  journal={Atherosclerosis},
  volume={223},
  number={2},
  pages={528},
  year={2012},
  publisher={Elsevier}
}

@article{liu2011dbnsfp,
  title={dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions},
  author={Liu, Xiaoming and Jian, Xueqiu and Boerwinkle, Eric},
  journal={Human mutation},
  volume={32},
  number={8},
  pages={894--899},
  year={2011},
  publisher={Wiley Online Library}
}

@article{schwarz2010mutationtaster,
  title={MutationTaster evaluates disease-causing potential of sequence alterations},
  author={Schwarz, Jana Marie and R{\"o}delsperger, Christian and Schuelke, Markus and Seelow, Dominik},
  journal={Nature methods},
  volume={7},
  number={8},
  pages={575--576},
  year={2010},
  publisher={Nature Publishing Group}
}

@article{wang2010annovar,
  title={ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data},
  author={Wang, Kai and Li, Mingyao and Hakonarson, Hakon},
  journal={Nucleic acids research},
  volume={38},
  number={16},
  pages={e164--e164},
  year={2010},
  publisher={Oxford Univ Press}
}

@article{altschul1997gapped,
  title={Gapped BLAST and PSI-BLAST: a new generation of protein database search programs},
  author={Altschul, Stephen F and Madden, Thomas L and Sch{\"a}ffer, Alejandro A and Zhang, Jinghui and Zhang, Zheng and Miller, Webb and Lipman, David J},
  journal={Nucleic acids research},
  volume={25},
  number={17},
  pages={3389--3402},
  year={1997},
  publisher={Oxford Univ Press}
}

@article{joosten2011series,
  title={A series of PDB related databases for everyday needs},
  author={Joosten, Robbie P and Te Beek, Tim AH and Krieger, Elmar and Hekkelman, Maarten L and Hooft, Rob WW and Schneider, Reinhard and Sander, Chris and Vriend, Gert},
  journal={Nucleic acids research},
  volume={39},
  number={suppl 1},
  pages={D411--D419},
  year={2011},
  publisher={Oxford Univ Press}
}

@article{berman2000protein,
  title={The protein data bank},
  author={Berman, Helen M and Westbrook, John and Feng, Zukang and Gilliland, Gary and Bhat, TN and Weissig, Helge and Shindyalov, Ilya N and Bourne, Philip E},
  journal={Nucleic acids research},
  volume={28},
  number={1},
  pages={235--242},
  year={2000},
  publisher={Oxford Univ Press}
}

@article{chapman2000biopython,
  title={Biopython: Python tools for computational biology},
  author={Chapman, Brad and Chang, Jeffrey},
  journal={ACM SIGBIO Newsletter},
  volume={20},
  number={2},
  pages={15--19},
  year={2000},
  publisher={ACM}
}

@article{pickrell2014epilepsy,
  title={EPILEPSY PREVALENCE, INCIDENCE AND SOCIOECONOMIC DEPRIVATION},
  author={Pickrell, Owen and Lacey, Arron and Bodger, Owen and Demmler, Joanne and Thomas, Rhys and Lyons, Ronan and Smith, Phil and Rees, Mark and Kerr, Mike},
  journal={Journal of Neurology, Neurosurgery \& Psychiatry},
  volume={85},
  number={10},
  pages={e4--e4},
  year={2014},
  publisher={BMJ Publishing Group Ltd}
}

@article{pickrell2014trends,
  title={Trends in the first antiepileptic drug prescribed for epilepsy between 2000 and 2010},
  author={Pickrell, W Owen and Lacey, Arron S and Thomas, Rhys H and Lyons, Ronan A and Smith, Phil EM and Rees, Mark I},
  journal={Seizure},
  volume={23},
  number={1},
  pages={77--80},
  year={2014},
  publisher={Elsevier}
}

@article{pickrell2012weight,
  title={Weight change associated with antiepileptic drugs},
  author={Pickrell, William Owen and Lacey, Arron S and Thomas, Rhys H and Smith, Philip EM and Rees, Mark I},
  journal={Journal of Neurology, Neurosurgery \& Psychiatry},
  pages={jnnp--2012},
  year={2012},
  publisher={BMJ Publishing Group Ltd}
}

有人能看出什么问题吗？正如我所说，一些参考资料确实有效（例如altschul1997gapped）。

答案1

我无法重现您报告的错误。不过，我确实注意到您的参考书目文件中有不少问题需要修复。

  • 最重要的是，在title田里，你需要小心不是让 BibTeX 将不应小写的单词小写。其中包括Wales(the country) 和 acrynonyms ( DNA, HGVbase) 等单词。

  • 有些作者是“企业作者”，例如，

    author={1000 Genomes Project Consortium and others},

    如果你不注意的话，第一作者会被 BibTeX 解释为名字为“1000”、“Genomes”和“Project”，姓氏为“Consortium”（因此被归类为 C 代表 Consortium！）。哎呀！你需要将此作者字段写为

    author={{1000 Genomes Project Consortium} and others}

    即，将整个第一作者的姓名放在一对额外的花括号中。同样，你需要写

    author={Green, Eric D and Guyer, Mark S and {National Human Genome Research Institute} and others},

  • 注意只使用关键字and，不要使用逗号来分隔作者。在带有关键字的条目中decode，您目前有

    author={Jeffrey R Gulcher, Kari Stefansson},

    根据 BibTeX 的语法规则，此条目将被解释为具有单身的作者的姓氏由三个单词组成（“Jeffrey R Gulcher”），名字有两个——“Kari”和“Stefansson”；因此，它也将被归类为“J”（代表“Jeffrey”），而不是“G”（代表“Gulcher”）。我认为这个字段应该

    author={Jeffrey R Gulcher and Kari Stefansson},

  • 您输入重音字符时表现非常出色，但 bib bile 中还存在一些其他非 7 位 ASCII 字符。例如，您需要将其替换—为---才能获得破折号。

  • 重复条目是没有意义的，对吧？因此，请删除键为 bromberg2007snap" 的条目的第二个实例。

  • 可选（未在下面的代码中实现）：我还会在缩写名字的末尾添加句点（“句号”），即写成Collins, Francis S. and Brooks, Lisa D.而不是Collins, Francis S and Brooks, Lisa D。如果您使用的参考书目样式恰好删除了句点，那也没关系。但是，据我所知，没有 bib 样式文件会添加如果缺少句号，则自动添加。

  • 介于可选和必需之间，但肯定非常可取（并且在下面的代码中也没有实现）：您应该尝试保持作者姓名信息在条目之间保持一致。例如，您有以下两个条目：

    @article{pickrell2014epilepsy,
  ...,
  author={Pickrell, Owen and Lacey, Arron and Bodger, Owen and Demmler, Joanne and Thomas, Rhys and Lyons, Ronan and Smith, Phil and Rees, Mark and Kerr, Mike},
  ...,
}

@article{pickrell2014trends,
  ...,
  author={Pickrell, W Owen and Lacey, Arron S and Thomas, Rhys H and Lyons, Ronan A and Smith, Phil EM and Rees, Mark I},
  ...,
}

    后一个条目提供了所有作者的中间名首字母，而前一个条目没有。为了避免混淆这些作者是否相同，您应该在前一个条目中提供缺失的信息。

\documentclass{article}
\usepackage{filecontents}
\begin{filecontents}{\jobname.bib}

@article{cargill1999characterization,
  title={Characterization of single-nucleotide polymorphisms in coding regions of human genes},
  author={Cargill, Michele and Altshuler, David and Ireland, James and Sklar, Pamela and Ardlie, Kristin and Patil, Nila and Lane, Charles R and Lim, Esther P and Kalyanaraman, Nilesh and Nemesh, James and others},
  journal={Nature genetics},
  volume={22},
  number={3},
  pages={231--238},
  year={1999},
  publisher={Nature Publishing Group}
}

@article{collins1998dna,
  title={A {DNA} polymorphism discovery resource for research on human genetic variation},
  author={Collins, Francis S and Brooks, Lisa D and Chakravarti, Aravinda},
  journal={Genome research},
  volume={8},
  number={12},
  pages={1229--1231},
  year={1998},
  publisher={Cold Spring Harbor Lab}
}

@article{frazer2009human,
  title={Human genetic variation and its contribution to complex traits},
  author={Frazer, Kelly A and Murray, Sarah S and Schork, Nicholas J and Topol, Eric J},
  journal={Nature Reviews Genetics},
  volume={10},
  number={4},
  pages={241--251},
  year={2009},
  publisher={Nature Publishing Group}
}

@article{10002010map,
  title={A map of human genome variation from population-scale sequencing},
  author={{1000 Genomes Project Consortium} and others},
  journal={Nature},
  volume={467},
  number={7319},
  pages={1061--1073},
  year={2010},
  publisher={Nature Publishing Group}
}

@article{smigielski2000dbsnp,
  title={{dbSNP}: a database of single nucleotide polymorphisms},
  author={Smigielski, Elizabeth M and Sirotkin, Karl and Ward, Minghong and Sherry, Stephen T},
  journal={Nucleic Acids Research},
  volume={28},
  number={1},
  pages={352--355},
  year={2000},
  publisher={Oxford Univ Press}
}

@article{fredman2002hgvbase,
  title={{HGVbase}: a human sequence variation database emphasizing data quality and a broad spectrum of data sources},
  author={Fredman, D and Siegfried, Marianne and Yuan, Yan P. and Bork, Peer and Lehv{\"a}slaiho, Heikki and Brookes, Anthony J},
  journal={Nucleic acids research},
  volume={30},
  number={1},
  pages={387--391},
  year={2002},
  publisher={Oxford Univ Press}
}

@article{hamosh2005online,
  title={{Online Mendelian Inheritance in Man (OMIM)}, a knowledgebase of human genes and genetic disorders},
  author={Hamosh, Ada and Scott, Alan F and Amberger, Joanna S and Bocchini, Carol A and McKusick, Victor A},
  journal={Nucleic acids research},
  volume={33},
  number={suppl 1},
  pages={D514--D517},
  year={2005},
  publisher={Oxford Univ Press}
}

@article{becker2004genetic,
  title={The genetic association database},
  author={Becker, Kevin G and Barnes, Kathleen C and Bright, Tiffani J and Wang, S Alex},
  journal={Nature genetics},
  volume={36},
  number={5},
  pages={431--432},
  year={2004},
  publisher={Nature Publishing Group}
}

@article{cooper1998human,
  title={The human gene mutation database},
  author={Cooper, David N and Ball, Edward V and Krawczak, Michael},
  journal={Nucleic acids research},
  volume={26},
  number={1},
  pages={285--287},
  year={1998},
  publisher={Oxford Univ Press}
}

@article{karolchik2003ucsc,
  title={The {UCSC} genome browser database},
  author={Karolchik, Donna and Baertsch, Robert and Diekhans, Mark and Furey, Terrence S. and Hinrichs, A and Lu, YT and Roskin, Krishna M. and Schwartz, M and Sugnet, Charles W. and Thomas, Daryl J and others},
  journal={Nucleic acids research},
  volume={31},
  number={1},
  pages={51--54},
  year={2003},
  publisher={Oxford Univ Press}
}

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\end{filecontents}
\bibliographystyle{plainnat}
\usepackage{natbib}

\begin{document}
\nocite{*}
\bibliography{\jobname}
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答案2

（这实际上是一条评论，但这样格式化更容易）

有重复

重复输入---文件x.bib的第208行：@article{bromberg2007snap

我尝试用这个 MWE 来举你缺失的参考例子

\documentclass{article}
\begin{document}    
\cite{altschul1997gapped}
\bibliographystyle{plain}
\bibliography{x}              %% to get x.bib
\end{document}

并且运行良好。请检查它是否适合您。

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