Alternatives and similar repositories for balancer-paper

Users that are interested in balancer-paper are comparing it to the libraries listed below

• dekkerlab / matrix_paper
  Scripts and notebooks used in Akgol Oksuz et al. paper
  ☆11Updated 4 years ago
• MarioniLab / CELLOseq
  Transposable element expression at unique loci in single cells with CELLO-seq
  ☆8Updated last year
• cyang235 / smooth-seq
  A pipeline for Smooth-seq data analysis.
  ☆10Updated 3 years ago
• daewoooo / StrandPhaseR
  R Package for phasing of single cell Strand-seq data
  ☆10Updated 6 months ago
• deWitLab / GENOVA
  GENome Organisation Visual Analytics
  ☆15Updated 3 years ago
• timplab / nanoNOMe
  nanoNOMe (Nucleosome Occupancy and Methylome nanopore sequencing) Analysis
  ☆18Updated 2 years ago
• shahcompbio / wgs
  Whole genome workflows
  ☆12Updated 8 months ago
• ay-lab / HiCnv
  HiCnv is used to call copy number variations and breakpoints from Hi-C data
  ☆21Updated last year
• UMCUGenetics / COLO829_somaticSV
  Scripts and files used in the generation of the COLO829 somatic SV truthset.
  ☆13Updated 3 years ago
• parklab / SCAN2
  SCAN2 is a somatic SNV and indel genotyper for single cells amplified by Primary Template-Directed Amplification (PTA)
  ☆13Updated 3 weeks ago
• emily-mitchell / normal_haematopoiesis
  ☆8Updated 2 years ago
• iaaaka / evo-devo
  ☆11Updated 4 years ago
• NYU-BFX / RNA-Seq_Standard
  ☆11Updated 6 years ago
• LappalainenLab / lorals_paper_code
  ☆26Updated 3 years ago
• VanLoo-lab / CAMDAC
  ☆12Updated last month
• sims-lab / CapCruncher
  Analysis tool for NG-Capture-C, Tri-C and Tiled-C data
  ☆9Updated 2 weeks ago
• gagneurlab / splicemap
  ☆21Updated 9 months ago
• EricSDavis / mariner
  Explore the Hi-Cs
  ☆11Updated last year
• XiaoTaoWang / StripeCaller
  A toolkit for analyzing architectural stripes
  ☆20Updated 7 months ago
• smlmbrt / SimilarityRegression
  Predicting TF sequence-specificity similarity with weighted alignments
  ☆13Updated 5 years ago
• amf71 / ECLIPSE
  ☆11Updated 2 years ago
• smithlabcode / abismal
  Abismal is a mapper of FASTQ bisulfite-converted short reads (between 50 and 1000 bases) to a FASTA reference genome.
  ☆18Updated this week
• oicr-gsi / sequenza
  Workflow for Sequenza, cellularity and ploidy
  ☆19Updated last month
• AmpliconSuite / AmpliconReconstructorOM
  Reconstructs complex variation using Bionano optical mapping data and breakpoint graph data
  ☆18Updated last year
• homeveg / nuctools
  software for analysis of chromatin feature occupancy profiles from high-throughput sequencing data
  ☆17Updated 5 years ago
• Gregor-Mendel-Institute / bookend
  End-guided RNA assembler
  ☆15Updated 3 months ago
• ChrisMaherLab / SV-Hotspot
  ☆9Updated 4 years ago
• JiejunShi / CAMDA
  Quantify the Concurrence of DNA Methylation and De-methylation
  ☆8Updated 3 years ago
• deWitLab / peakC
  Peak calling for 4C data
  ☆12Updated 7 years ago
• heinc1010 / BAMixChecker
  BAMixChecker: A fast and efficient tool for sample matching checkup
  ☆14Updated 3 years ago