Marcel H. Schulz

Molecular Biology · 2008–2018

A researcher in the Science corpus: 5 papers; trusts 2 researchers and is trusted by 5 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 61 citations into it; #7,921 of 17,773 by trust here, #2,878 by citations
• Artificial Intelligence — 10 citations into it
• Information Systems — 5 citations into it

Whom Marcel H. Schulz trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. W. James Kent
2. Eugene W. Myers
3. Peter M. Rice
4. Ali Mortazavi
5. Jason D. Buenrostro
6. M. Guttman
7. Inanç Birol
8. ENCODEConsortium
9. Jason Ernst
10. Manfred G. Grabherr

Who trusts Marcel H. Schulz overall

1. Brian J. Haas
2. Kimberly R. Kukurba
3. N. Davidson
4. Alicia Oshlack
5. Shiyuyun Tang
6. Daniel C. Koboldt
7. M. Rius
8. Elena Bushmanova
9. Richard D. Smith-Unna
10. Ana Conesa

Papers from Marcel H. Schulz's perspective

Ordered by how strongly the researchers Marcel H. Schulz trusts endorse each paper. Same corpus, a different order for every researcher.

1. BLAT--the BLAST-like alignment tool. (Genome Research)
2. Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
3. Velvet: algorithms for de novo short read assembly using de Bruijn graphs.
4. De novo transcriptome assembly with ABySS (Bioinform.)
5. Statistical inferences for isoform expression in RNA-Seq (Bioinform.)
6. The Sequence Alignment/Map format and SAMtools (Bioinform.)
7. EMBOSS: the European Molecular Biology Open Software Suite.
8. Single-cell chromatin accessibility reveals principles of regulatory variation (Nature)
9. A Global View of Gene Activity and Alternative Splicing by Deep Sequencing of the Human Transcriptome (Science)
10. The fragment assembly string graph (ECCB/JBI)

Their papers

• A Global View of Gene Activity and Alternative Splicing by Deep Sequencing of the Human Transcriptome (2008) — 1,338 citations
• Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads (2009) — 2,074 citations
• Oases: robust de novo RNA-seq assembly across the dynamic range of expression levels (2012) — 1,459 citations
• Clinical diagnostics in human genetics with semantic similarity searches in ontologies. (2009) — 542 citations
• Identification of transcription factor binding sites using ATAC-seq (2018) — 393 citations