Modeling, validation and verification of three-dimensional cell-scaffold contacts from terabyte-sized images.

Abstract:

BACKGROUND:Cell-scaffold contact measurements are derived from pairs of co-registered volumetric fluorescent confocal laser scanning microscopy (CLSM) images (z-stacks) of stained cells and three types of scaffolds (i.e., spun coat, large microfiber, and medium microfiber). Our analysis of the acquired terabyte-sized collection is motivated by the need to understand the nature of the shape dimensionality (1D vs 2D vs 3D) of cell-scaffold interactions relevant to tissue engineers that grow cells on biomaterial scaffolds. RESULTS:We designed five statistical and three geometrical contact models, and then down-selected them to one from each category using a validation approach based on physically orthogonal measurements to CLSM. The two selected models were applied to 414 z-stacks with three scaffold types and all contact results were visually verified. A planar geometrical model for the spun coat scaffold type was validated from atomic force microscopy images by computing surface roughness of 52.35 nm ±31.76 nm which was 2 to 8 times smaller than the CLSM resolution. A cylindrical model for fiber scaffolds was validated from multi-view 2D scanning electron microscopy (SEM) images. The fiber scaffold segmentation error was assessed by comparing fiber diameters from SEM and CLSM to be between 0.46% to 3.8% of the SEM reference values. For contact verification, we constructed a web-based visual verification system with 414 pairs of images with cells and their segmentation results, and with 4968 movies with animated cell, scaffold, and contact overlays. Based on visual verification by three experts, we report the accuracy of cell segmentation to be 96.4% with 94.3% precision, and the accuracy of cell-scaffold contact for a statistical model to be 62.6% with 76.7% precision and for a geometrical model to be 93.5% with 87.6% precision. CONCLUSIONS:The novelty of our approach lies in (1) representing cell-scaffold contact sites with statistical intensity and geometrical shape models, (2) designing a methodology for validating 3D geometrical contact models and (3) devising a mechanism for visual verification of hundreds of 3D measurements. The raw and processed data are publicly available from https://isg.nist.gov/deepzoomweb/data/ together with the web -based verification system.

journal_name

BMC Bioinformatics

journal_title

BMC bioinformatics

authors

Bajcsy P,Yoon S,Florczyk SJ,Hotaling NA,Simon M,Szczypinski PM,Schaub NJ,Simon CG Jr,Brady M,Sriram RD

doi

10.1186/s12859-017-1928-x

subject

Has Abstract

pub_date

2017-11-28 00:00:00

pages

526

issue

1

issn

1471-2105

pii

10.1186/s12859-017-1928-x

journal_volume

18

pub_type

杂志文章
  • SEQprocess: a modularized and customizable pipeline framework for NGS processing in R package.

    abstract:BACKGROUNDS:Next-Generation Sequencing (NGS) is now widely used in biomedical research for various applications. Processing of NGS data requires multiple programs and customization of the processing pipelines according to the data platforms. However, rapid progress of the NGS applications and processing methods urgentl...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-019-2676-x

    authors: Joo T,Choi JH,Lee JH,Park SE,Jeon Y,Jung SH,Woo HG

    更新日期:2019-02-20 00:00:00

  • Odyssey: a semi-automated pipeline for phasing, imputation, and analysis of genome-wide genetic data.

    abstract:BACKGROUND:Genome imputation, admixture resolution and genome-wide association analyses are timely and computationally intensive processes with many composite and requisite steps. Analysis time increases further when building and installing the run programs required for these analyses. For scientists that may not be as...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-019-2964-5

    authors: Eller RJ,Janga SC,Walsh S

    更新日期:2019-06-28 00:00:00

  • Bison: bisulfite alignment on nodes of a cluster.

    abstract:BACKGROUND:DNA methylation changes are associated with a wide array of biological processes. Bisulfite conversion of DNA followed by high-throughput sequencing is increasingly being used to assess genome-wide methylation at single-base resolution. The relative slowness of most commonly used aligners for processing such...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-15-337

    authors: Ryan DP,Ehninger D

    更新日期:2014-10-18 00:00:00

  • BCDForest: a boosting cascade deep forest model towards the classification of cancer subtypes based on gene expression data.

    abstract:BACKGROUND:The classification of cancer subtypes is of great importance to cancer disease diagnosis and therapy. Many supervised learning approaches have been applied to cancer subtype classification in the past few years, especially of deep learning based approaches. Recently, the deep forest model has been proposed a...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-018-2095-4

    authors: Guo Y,Liu S,Li Z,Shang X

    更新日期:2018-04-11 00:00:00

  • RocSampler: regularizing overlapping protein complexes in protein-protein interaction networks.

    abstract:BACKGROUND:In recent years, protein-protein interaction (PPI) networks have been well recognized as important resources to elucidate various biological processes and cellular mechanisms. In this paper, we address the problem of predicting protein complexes from a PPI network. This problem has two difficulties. One is r...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-017-1920-5

    authors: Maruyama O,Kuwahara Y

    更新日期:2017-12-06 00:00:00

  • In silico design of targeted SRM-based experiments.

    abstract::Selected reaction monitoring (SRM)-based proteomics approaches enable highly sensitive and reproducible assays for profiling of thousands of peptides in one experiment. The development of such assays involves the determination of retention time, detectability and fragmentation properties of peptides, followed by an op...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-13-S16-S8

    authors: Nahnsen S,Kohlbacher O

    更新日期:2012-01-01 00:00:00

  • Robust sequence alignment using evolutionary rates coupled with an amino acid substitution matrix.

    abstract:BACKGROUND:Selective pressures at the DNA level shape genes into profiles consisting of patterns of rapidly evolving sites and sites withstanding change. These profiles remain detectable even when protein sequences become extensively diverged. A common task in molecular biology is to infer functional, structural or evo...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-015-0688-8

    authors: Ndhlovu A,Hazelhurst S,Durand PM

    更新日期:2015-08-14 00:00:00

  • circRNAprofiler: an R-based computational framework for the downstream analysis of circular RNAs.

    abstract:BACKGROUND:Circular RNAs (circRNAs) are a newly appreciated class of non-coding RNA molecules. Numerous tools have been developed for the detection of circRNAs, however computational tools to perform downstream functional analysis of circRNAs are scarce. RESULTS:We present circRNAprofiler, an R-based computational fra...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-020-3500-3

    authors: Aufiero S,Reckman YJ,Tijsen AJ,Pinto YM,Creemers EE

    更新日期:2020-04-29 00:00:00

  • PVT: an efficient computational procedure to speed up next-generation sequence analysis.

    abstract:BACKGROUND:High-throughput Next-Generation Sequencing (NGS) techniques are advancing genomics and molecular biology research. This technology generates substantially large data which puts up a major challenge to the scientists for an efficient, cost and time effective solution to analyse such data. Further, for the dif...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-15-167

    authors: Maji RK,Sarkar A,Khatua S,Dasgupta S,Ghosh Z

    更新日期:2014-06-04 00:00:00

  • GSV: a web-based genome synteny viewer for customized data.

    abstract:BACKGROUND:The analysis of genome synteny is a common practice in comparative genomics. With the advent of DNA sequencing technologies, individual biologists can rapidly produce their genomic sequences of interest. Although web-based synteny visualization tools are convenient for biologists to use, none of the existing...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-12-316

    authors: Revanna KV,Chiu CC,Bierschank E,Dong Q

    更新日期:2011-08-02 00:00:00

  • The InDeVal insertion/deletion evaluation tool: a program for finding target regions in DNA sequences and for aiding in sequence comparison.

    abstract:BACKGROUND:The program InDeVal was originally developed to help researchers find known regions of insertion/deletion activity (with the exception of isolated single-base indels) in newly determined Poaceae trnL-F sequences and compare them with 533 previously determined sequences. It is supplied with input files design...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-5-173

    authors: Stoneberg Holt SD,Holt JA

    更新日期:2004-10-29 00:00:00

  • Correction to: Effective machine-learning assembly for next-generation amplicon sequencing with very low coverage.

    abstract::Following publication of the original article [1], the author reported that there are several errors in the original article. ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章,已发布勘误

    doi:10.1186/s12859-019-3318-z

    authors: Ranjard L,Wong TKF,Rodrigo AG

    更新日期:2020-01-22 00:00:00

  • PanACEA: a bioinformatics tool for the exploration and visualization of bacterial pan-chromosomes.

    abstract:BACKGROUND:Bacterial pan-genomes, comprised of conserved and variable genes across multiple sequenced bacterial genomes, allow for identification of genomic regions that are phylogenetically discriminating or functionally important. Pan-genomes consist of large amounts of data, which can restrict researchers ability to...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-018-2250-y

    authors: Clarke TH,Brinkac LM,Inman JM,Sutton G,Fouts DE

    更新日期:2018-06-27 00:00:00

  • Knowledge-based variable selection for learning rules from proteomic data.

    abstract:BACKGROUND:The incorporation of biological knowledge can enhance the analysis of biomedical data. We present a novel method that uses a proteomic knowledge base to enhance the performance of a rule-learning algorithm in identifying putative biomarkers of disease from high-dimensional proteomic mass spectral data. In pa...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-10-S9-S16

    authors: Lustgarten JL,Visweswaran S,Bowser RP,Hogan WR,Gopalakrishnan V

    更新日期:2009-09-17 00:00:00

  • Evaluation of high-throughput functional categorization of human disease genes.

    abstract:BACKGROUND:Biological data that are well-organized by an ontology, such as Gene Ontology, enables high-throughput availability of the semantic web. It can also be used to facilitate high throughput classification of biomedical information. However, to our knowledge, no evaluation has been published on automating classi...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-8-S3-S7

    authors: Chen JL,Liu Y,Sam LT,Li J,Lussier YA

    更新日期:2007-05-09 00:00:00

  • Identifications of conserved 7-mers in 3'-UTRs and microRNAs in Drosophila.

    abstract:BACKGROUND:MicroRNAs (miRNAs) are a class of endogenous regulatory small RNAs which play an important role in posttranscriptional regulations by targeting mRNAs for cleavage or translational repression. The base-pairing between the 5'-end of miRNA and the target mRNA 3'-UTRs is essential for the miRNA:mRNA recognition....

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-8-432

    authors: Gu J,Fu H,Zhang X,Li Y

    更新日期:2007-11-08 00:00:00

  • A new advance in alternative splicing databases: from catalogue to detailed analysis of regulation of expression and function of human alternative splicing variants.

    abstract:BACKGROUND:Most human genes produce several transcripts with different exon contents by using alternative promoters, alternative polyadenylation sites and alternative splice sites. Much effort has been devoted to describing known gene transcripts through the development of numerous databases. Nevertheless, owing to the...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-8-180

    authors: de la Grange P,Dutertre M,Correa M,Auboeuf D

    更新日期:2007-06-04 00:00:00

  • Comparison of methods to detect copy number alterations in cancer using simulated and real genotyping data.

    abstract:BACKGROUND:The detection of genomic copy number alterations (CNA) in cancer based on SNP arrays requires methods that take into account tumour specific factors such as normal cell contamination and tumour heterogeneity. A number of tools have been recently developed but their performance needs yet to be thoroughly asse...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-13-192

    authors: Mosén-Ansorena D,Aransay AM,Rodríguez-Ezpeleta N

    更新日期:2012-08-07 00:00:00

  • Rule-based knowledge aggregation for large-scale protein sequence analysis of influenza A viruses.

    abstract:BACKGROUND:The explosive growth of biological data provides opportunities for new statistical and comparative analyses of large information sets, such as alignments comprising tens of thousands of sequences. In such studies, sequence annotations frequently play an essential role, and reliable results depend on metadata...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-9-S1-S7

    authors: Miotto O,Tan TW,Brusic V

    更新日期:2008-01-01 00:00:00

  • Integrating diverse biological and computational sources for reliable protein-protein interactions.

    abstract:BACKGROUND:Protein-protein interactions (PPIs) play important roles in various cellular processes. However, the low quality of current PPI data detected from high-throughput screening techniques has diminished the potential usefulness of the data. We need to develop a method to address the high data noise and incomplet...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-11-S7-S8

    authors: Wu M,Li X,Chua HN,Kwoh CK,Ng SK

    更新日期:2010-10-15 00:00:00

  • TE-Tracker: systematic identification of transposition events through whole-genome resequencing.

    abstract:BACKGROUND:Transposable elements (TEs) are DNA sequences that are able to move from their location in the genome by cutting or copying themselves to another locus. As such, they are increasingly recognized as impacting all aspects of genome function. With the dramatic reduction in cost of DNA sequencing, it is now poss...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-014-0377-z

    authors: Gilly A,Etcheverry M,Madoui MA,Guy J,Quadrana L,Alberti A,Martin A,Heitkam T,Engelen S,Labadie K,Le Pen J,Wincker P,Colot V,Aury JM

    更新日期:2014-11-19 00:00:00

  • Distilling structure in Taverna scientific workflows: a refactoring approach.

    abstract:BACKGROUND:Scientific workflows management systems are increasingly used to specify and manage bioinformatics experiments. Their programming model appeals to bioinformaticians, who can use them to easily specify complex data processing pipelines. Such a model is underpinned by a graph structure, where nodes represent b...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-15-S1-S12

    authors: Cohen-Boulakia S,Chen J,Missier P,Goble C,Williams AR,Froidevaux C

    更新日期:2014-01-01 00:00:00

  • The identification of informative genes from multiple datasets with increasing complexity.

    abstract:BACKGROUND:In microarray data analysis, factors such as data quality, biological variation, and the increasingly multi-layered nature of more complex biological systems complicates the modelling of regulatory networks that can represent and capture the interactions among genes. We believe that the use of multiple datas...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-11-32

    authors: Anvar SY,'t Hoen PA,Tucker A

    更新日期:2010-01-15 00:00:00

  • Identification of novel alternative splicing biomarkers for breast cancer with LC/MS/MS and RNA-Seq.

    abstract:BACKGROUND:Alternative splicing isoforms have been reported as a new and robust class of diagnostic biomarkers. Over 95% of human genes are estimated to be alternatively spliced as a powerful means of producing functionally diverse proteins from a single gene. The emergence of next-generation sequencing technologies, e...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-020-03824-8

    authors: Zhang F,Deng CK,Wang M,Deng B,Barber R,Huang G

    更新日期:2020-12-03 00:00:00

  • Sigma-RF: prediction of the variability of spatial restraints in template-based modeling by random forest.

    abstract:BACKGROUND:In template-based modeling when using a single template, inter-atomic distances of an unknown protein structure are assumed to be distributed by Gaussian probability density functions, whose center peaks are located at the distances between corresponding atoms in the template structure. The width of the Gaus...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-015-0526-z

    authors: Lee J,Lee K,Joung I,Joo K,Brooks BR,Lee J

    更新日期:2015-03-21 00:00:00

  • Evidence for intron length conservation in a set of mammalian genes associated with embryonic development.

    abstract:BACKGROUND:We carried out an analysis of intron length conservation across a diverse group of nineteen mammalian species. Motivated by recent research suggesting a role for time delays associated with intron transcription in gene expression oscillations required for early embryonic patterning, we searched for examples ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-12-S9-S16

    authors: Seoighe C,Korir PK

    更新日期:2011-10-05 00:00:00

  • Integrated olfactory receptor and microarray gene expression databases.

    abstract:BACKGROUND:Gene expression patterns of olfactory receptors (ORs) are an important component of the signal encoding mechanism in the olfactory system since they determine the interactions between odorant ligands and sensory neurons. We have developed the Olfactory Receptor Microarray Database (ORMD) to house OR gene exp...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-8-231

    authors: Liu N,Crasto CJ,Ma M

    更新日期:2007-06-30 00:00:00

  • Sparse multiple co-Inertia analysis with application to integrative analysis of multi -Omics data.

    abstract:BACKGROUND:Multiple co-inertia analysis (mCIA) is a multivariate analysis method that can assess relationships and trends in multiple datasets. Recently it has been used for integrative analysis of multiple high-dimensional -omics datasets. However, its estimated loading vectors are non-sparse, which presents challenge...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-020-3455-4

    authors: Min EJ,Long Q

    更新日期:2020-04-15 00:00:00

  • Can Zipf's law be adapted to normalize microarrays?

    abstract:BACKGROUND:Normalization is the process of removing non-biological sources of variation between array experiments. Recent investigations of data in gene expression databases for varying organisms and tissues have shown that the majority of expressed genes exhibit a power-law distribution with an exponent close to -1 (i...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-6-37

    authors: Lu T,Costello CM,Croucher PJ,Häsler R,Deuschl G,Schreiber S

    更新日期:2005-02-23 00:00:00

  • Cloning, analysis and functional annotation of expressed sequence tags from the Earthworm Eisenia fetida.

    abstract:BACKGROUND:Eisenia fetida, commonly known as red wiggler or compost worm, belongs to the Lumbricidae family of the Annelida phylum. Little is known about its genome sequence although it has been extensively used as a test organism in terrestrial ecotoxicology. In order to understand its gene expression response to envi...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-8-S7-S7

    authors: Pirooznia M,Gong P,Guan X,Inouye LS,Yang K,Perkins EJ,Deng Y

    更新日期:2007-11-01 00:00:00