Marcel Martin

Q: What Schools Are Affiliated With Marcel Martin

Marcel Martin is affiliated with the following schools: University of California, Berkeley, Stanford University

Marcel Martin's AcademicInfluence.com Rankings

Marcel Martin

Computer Science

#9101

World Rank

#9564

Historical Rank

Computational Linguistics

#2148

World Rank

#2170

Historical Rank

Machine Learning

#3903

World Rank

#3950

Historical Rank

Artificial Intelligence

#4235

World Rank

#4294

Historical Rank

computer-science Degrees

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Computer Science

Marcel Martin's Degrees

PhD Computer Science Stanford University
Masters Computer Science University of California, Berkeley
Bachelors Computer Science University of California, Berkeley

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Marcel Martin's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Cutadapt removes adapter sequences from high-throughput sequencing reads (2011) (18335)
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3 (2013) (413)
WhatsHap: fast and accurate read-based phasing (2016) (207)
Deep sequencing reveals differential expression of microRNAs in favorable versus unfavorable neuroblastoma (2010) (190)
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling. (2013) (176)
Atropos: specific, sensitive, and speedy trimming of sequencing reads (2017) (159)
Production of individualized V gene databases reveals high levels of immunoglobulin genetic diversity (2016) (151)
Computational pan-genomics: status, promises and challenges (2016) (145)
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population (2017) (136)
The genetic basis for ecological adaptation of the Atlantic herring revealed by genome sequencing (2016) (126)
Concomitant p53 gene mutation and increased radiosensitivity in rat lung embryo epithelial cells during neoplastic development. (1994) (102)
Cloche is a bHLH-PAS transcription factor that drives haemato-vascular specification (2016) (94)
Discovering motifs that induce sequencing errors (2013) (70)
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability (2019) (70)
Exact and heuristic algorithms for weighted cluster editing. (2007) (69)
Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants (2018) (51)
Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations (2013) (48)
The SEQanswers wiki: a wiki database of tools for high-throughput sequencing analysis (2011) (45)
De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data (2018) (44)
High-Quality Library Preparation for NGS-Based Immunoglobulin Germline Gene Inference and Repertoire Expression Analysis (2019) (41)
Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incomplete. (2009) (41)
Bioconda: sustainable and comprehensive software distribution for the life sciences (2017) (40)
Cloche is a bHLH-PAS transcription factor that drives haemato-vascular specification (2018) (37)
Read-based phasing of related individuals (2016) (36)
Loss of heterozygosity events impeding breast cancer metastasis contain the MTA1 gene. (2001) (34)
Next‐generation RNA sequencing reveals differential expression of MYCN target genes and suggests the mTOR pathway as a promising therapy target in MYCN‐amplified neuroblastoma (2013) (33)
Amplikyzer: Automated methylation analysis of amplicons from bisulfite flowgram sequencing (2013) (30)
Exon-level expression analyses identify MYCN and NTRK1 as major determinants of alternative exon usage and robustly predict primary neuroblastoma outcome (2012) (26)
Clonal relations in the mouse brain revealed by single-cell and spatial transcriptomics (2021) (25)
DECOMP - from interpreting Mass Spectrometry peaks to solving the Money Changing Problem (2008) (24)
Recognition of Manual Actions Using Vector Quantization and Dynamic Time Warping (2010) (19)
Extensive dissemination and intraclonal maturation of HIV Env vaccine-induced B cell responses (2019) (18)
Identifying transcriptional miRNA biomarkers by integrating high-throughput sequencing and real-time PCR data. (2013) (13)
Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants. (2020) (10)
From cutadapt to sequencetools (sqt): a versatile toolset for sequencing projects (2012) (8)
HapCHAT: adaptive haplotype assembly for efficiently leveraging high coverage in long reads (2017) (8)
Clonally heritable gene expression imparts a layer of diversity within cell types (2022) (8)
Algorithms and tools for the analysis of high throughput DNA sequencing data (2014) (6)
Author response: The genetic basis for ecological adaptation of the Atlantic herring revealed by genome sequencing (2016) (6)
Aligning Flowgrams to DNA Sequences (2013) (3)
minute: A MINUTE-ChIP data analysis workflow (2022) (2)
Deep sequencing of the small-RNA transcriptome reveals differenzial expression of microRNAs in high-risk versus low-risk neuroblastoma (2010) (1)
Discovering motifs that induce sequencing errors (2013) (1)
A BWT-Based Suffix Array Construction (2009) (1)
Read-Based Phasing and Analysis of Phased Variants with WhatsHap. (2023) (1)
From cytogenetics to cytogenomics whole genome sequencing as a comprehensive genetic test in rare disease diagnostics (2019) (1)
A symbol-oriented approach to motion analysis (2009) (0)
The Coffin-Siris and Nicolaides Baraitser syndromes – clinical phenotypes of 43 prerviously unreported patients and mutational spectrum of the SWI/SNF complex (2012) (0)
trimming of sequencing reads 2 (2017) (0)
Exon-level gene expression analyses of primary neuroblastoma improves risk prediction and identifies JARID1C as a candidate target (2009) (0)
Abstract P6-13-18: Triple-negative kinase profile guides in the selection of the multi-kinase inhibitor EC70124 as an active antitumor agent (2016) (0)
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability (2019) (0)

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What Schools Are Affiliated With Marcel Martin?

Marcel Martin is affiliated with the following schools:

Marcel Martin's Academic­Influence.com Rankings

Marcel Martin's Degrees

Similar Degrees You Can Earn

Why Is Marcel Martin Influential?

Marcel Martin's Published Works

Published Works

What Schools Are Affiliated With Marcel Martin?

Marcel Martin's AcademicInfluence.com Rankings