| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
A short history of SHELX.
|
Acta Crystallogr A
|
2007
|
7339.18
|
|
2
|
Structure validation in chemical crystallography.
|
Acta Crystallogr D Biol Crystallogr
|
2009
|
1216.15
|
|
3
|
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.
|
Genome Biol
|
2009
|
235.12
|
|
4
|
The Sequence Alignment/Map format and SAMtools.
|
Bioinformatics
|
2009
|
232.39
|
|
5
|
MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods.
|
Mol Biol Evol
|
2011
|
220.97
|
|
6
|
PLINK: a tool set for whole-genome association and population-based linkage analyses.
|
Am J Hum Genet
|
2007
|
209.92
|
|
7
|
Fast and accurate short read alignment with Burrows-Wheeler transform.
|
Bioinformatics
|
2009
|
190.94
|
|
8
|
Global cancer statistics.
|
CA Cancer J Clin
|
2011
|
185.92
|
|
9
|
The RAST Server: rapid annotations using subsystems technology.
|
BMC Genomics
|
2008
|
175.18
|
|
10
|
MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0.
|
Mol Biol Evol
|
2007
|
168.76
|
|
11
|
Crystal structure refinement with SHELXL.
|
Acta Crystallogr C Struct Chem
|
2015
|
158.65
|
|
12
|
Mapping short DNA sequencing reads and calling variants using mapping quality scores.
|
Genome Res
|
2008
|
157.44
|
|
13
|
Velvet: algorithms for de novo short read assembly using de Bruijn graphs.
|
Genome Res
|
2008
|
151.16
|
|
14
|
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
Nature
|
2007
|
144.95
|
|
15
|
Hallmarks of cancer: the next generation.
|
Cell
|
2011
|
140.01
|
|
16
|
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources.
|
Nat Protoc
|
2009
|
137.99
|
|
17
|
Mapping and quantifying mammalian transcriptomes by RNA-Seq.
|
Nat Methods
|
2008
|
126.81
|
|
18
|
Clustal W and Clustal X version 2.0.
|
Bioinformatics
|
2007
|
126.47
|
|
19
|
A map of human genome variation from population-scale sequencing.
|
Nature
|
2010
|
121.13
|
|
20
|
MEGA6: Molecular Evolutionary Genetics Analysis version 6.0.
|
Mol Biol Evol
|
2013
|
112.81
|
|
21
|
PHENIX: a comprehensive Python-based system for macromolecular structure solution.
|
Acta Crystallogr D Biol Crystallogr
|
2010
|
108.52
|
|
22
|
Phaser crystallographic software.
|
J Appl Crystallogr
|
2007
|
108.34
|
|
23
|
Cancer statistics, 2010.
|
CA Cancer J Clin
|
2010
|
103.28
|
|
24
|
Induction of pluripotent stem cells from adult human fibroblasts by defined factors.
|
Cell
|
2007
|
101.42
|
|
25
|
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
|
Genome Res
|
2010
|
97.51
|
|
26
|
MicroRNAs: target recognition and regulatory functions.
|
Cell
|
2009
|
92.17
|
|
27
|
Accurate whole human genome sequencing using reversible terminator chemistry.
|
Nature
|
2008
|
90.20
|
|
28
|
Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008.
|
Int J Cancer
|
2010
|
90.16
|
|
29
|
Features and development of Coot.
|
Acta Crystallogr D Biol Crystallogr
|
2010
|
89.46
|
|
30
|
Cancer statistics, 2012.
|
CA Cancer J Clin
|
2012
|
87.38
|
|
31
|
Cancer statistics, 2008.
|
CA Cancer J Clin
|
2008
|
86.74
|
|
32
|
RNAmmer: consistent and rapid annotation of ribosomal RNA genes.
|
Nucleic Acids Res
|
2007
|
85.81
|
|
33
|
High-resolution profiling of histone methylations in the human genome.
|
Cell
|
2007
|
85.74
|
|
34
|
A second generation human haplotype map of over 3.1 million SNPs.
|
Nature
|
2007
|
85.39
|
|
35
|
QIIME allows analysis of high-throughput community sequencing data.
|
Nat Methods
|
2010
|
85.34
|
|
36
|
Cancer statistics, 2013.
|
CA Cancer J Clin
|
2013
|
84.72
|
|
37
|
Determination of absolute structure using Bayesian statistics on Bijvoet differences.
|
J Appl Crystallogr
|
2008
|
84.57
|
|
38
|
NIH Image to ImageJ: 25 years of image analysis.
|
Nat Methods
|
2012
|
84.41
|
|
39
|
Fast gapped-read alignment with Bowtie 2.
|
Nat Methods
|
2012
|
83.79
|
|
40
|
Cancer statistics, 2009.
|
CA Cancer J Clin
|
2009
|
83.57
|
|
41
|
TopHat: discovering splice junctions with RNA-Seq.
|
Bioinformatics
|
2009
|
81.13
|
|
42
|
A method and server for predicting damaging missense mutations.
|
Nat Methods
|
2010
|
78.53
|
|
43
|
New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1).
|
Eur J Cancer
|
2009
|
77.71
|
|
44
|
Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities.
|
Appl Environ Microbiol
|
2009
|
77.55
|
|
45
|
Comprehensive genomic characterization defines human glioblastoma genes and core pathways.
|
Nature
|
2008
|
75.40
|
|
46
|
Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation.
|
Nat Biotechnol
|
2010
|
75.21
|
|
47
|
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.
|
Nature
|
2007
|
75.09
|
|
48
|
BEAST: Bayesian evolutionary analysis by sampling trees.
|
BMC Evol Biol
|
2007
|
74.13
|
|
49
|
Cancer statistics, 2014.
|
CA Cancer J Clin
|
2014
|
72.81
|
|
50
|
Induced pluripotent stem cell lines derived from human somatic cells.
|
Science
|
2007
|
71.50
|