ライフサイエンスコーパス: intergenic

1 Ss) were annotated as noncoding, with 24% in intergenic, 12% in promoters, and 28% in introns, with s

2 Here, we find that the exonisation of intergenic Alu elements introduced new terminal exons an

3 On the mechanistic level, we show that intergenic Alu exonisation can compete both with alterna

4 essing of preceding genes, and elucidate how intergenic Alu exonisation can contribute to tissue-spec

5 The majority of association signals are intergenic and evidence is accumulating that a high prop

6 lly greatest in silent or weakly transcribed intergenic and genic regions and accompanied by an incre

7 protein-coding hosts or neighbours, some are intergenic and independent.

8 Intergenic and intragenic enhancers found inside topolog

9 c acid, and parathyroid hormone through both intergenic and intronic enhancers.

10 For some cell types intergenic and intronic targets were more frequent where

11 BMI1 was highly enriched at intergenic and pericentric heterochromatin, co-immunopre

12 yses found biases toward high GC content and intergenic and repetitive regions.

13 ancer chromatin regions distal to MYOD1 were intergenic and up to 19 kb long.

14 to identify 4 riboswitches, 13 trans-acting (intergenic), and 22 cis-acting (antisense) small RNAs (t

15 s in different regions of the genome (genic, intergenic, and heterochromatic) and at different distan

16 IC in the 4p16.1 region located mostly in an intergenic area near SLC2A9 that were not driven by link

17 DNA is preferentially hypomethylated within intergenic areas and LINE1 promoter areas of the genome.

18 very group; P=0.00031 replication group), is intergenic between HLA-DRA and BTNL2.

19 xclusion of small intronic deletions left 33 intergenic breaks in G089 and 14 in PC346C.

20 We report a novel intergenic breast cancer risk locus containing an enhanc

21 ant loss of SUMOylation occurred at inactive intergenic chromatin regions that were associated with C

22 n (PCR) analyses: Enterobacterial Repetitive Intergenic Consensus (ERIC) and Random Amplified Polymor

23 irms the previous enterobacterial repetitive intergenic consensus (ERIC)-polymerase chain reaction (P

24 The intergenic control region 1 (IGCR1) in the V(H)-to-D int

25 f methylation in the heart, enriched in lone intergenic CpGs and depleted from CpG islands around gen

26 tissues requires assessment of understudied intergenic CpGs distal to gene promoters to reveal the f

27 ogenic activity of AID leading to intra- and intergenic deletions via homologous recombination of seq

28 In a set of 104 gold standard intergenic deletions, our method achieved a sensitivity

29 operon variants with systematically modified intergenic distances and upstream translation rates.

30 of marker genes with operon prediction using intergenic distances, and queries to the carbohydrate-ac

31 schemes to obtain the best performance over intergenic DNA sequence data.

32 ensities of H3K27me3 covering both genes and intergenic DNA, together with very low levels of the rep

33 In summary, we demonstrate that intergenic elements can affect processing of preceding g

34 dent on high STAT5 levels as a result of the intergenic enhancer.

35 400Kb upstream to IGFBP5, which overlaps an intergenic ERalpha-bound enhancer that loops to the IGFB

36 kpoints were partitioned into intragenic and intergenic events.

37 ssays demonstrated that hGRbeta binds to the intergenic glucocorticoid response element (GRE) of the

38 ers lack H3K27me3, and it is unknown whether intergenic H3K27me3 deposits affect nearby genes.

39 Excess intergenic H3K27me3 in both TF-deficient tissues is asso

40 e an epigenomic framework for barley whereby intergenic H3K27me3 specifies facultative heterochromati

41 lti-exonic transcripts from 561 intronic and intergenic haploblocks associated with 392 traits and di

42 unique sequence derived from the prrF1-prrF2 intergenic (IG) sequence (the PrrHIG sequence).

43 negatively impacted or increased by the HN-L intergenic insertion.

44 ell predominantly within introns, exons, and intergenic intervals, while showing a significant deplet

45 We focused on the long intergenic/intervening ncRNAs (lincRNAs), hidden within

46 The intergenic IRES of Cricket Paralysis Virus (CrPV-IRES) f

47 nal significance of this region, which being intergenic is probably regulatory.

48 dicted in Trichodesmium, when normalized per intergenic kilobase, was comparable and twofold higher t

49 ECONEXIN was the most highly conserved intergenic lncRNA containing 83.0% homology with the mou

50 Given that intergenic lncRNA have substantially less sequence conse

51 requirements for nuclear localization in an intergenic lncRNA named BORG (BMP2-OP1-responsive gene),

52 an experimental reannotation of the GENCODE intergenic lncRNA populations in matched human and mouse

53 The current study identified a novel intergenic lncRNA, LINC00461 (ECONEXIN) using a combined

54 genes across species, evolutionary conserved intergenic lncRNAs are likely to be functional.

55 ification of these lncRNAs reveals that most intergenic lncRNAs originate from enhancers rather than

56 For this study, hundreds of intergenic LncRNAs were identified that are expressed in

57 ic class of RNAs that includes, for example, intergenic lncRNAs, antisense transcripts, and enhancer

58 med strong hypoxia-dependent activation of 2 intergenic lncRNAs: LINC00323 and MIR503HG.

59 atterns, and uncovers two notable classes of intergenic lncRNAs: one showing strong purifying selecti

60 Modeling a gene's expression from its intergenic locus and trans-regulatory context is a funda

61 Unexpectedly, we observed an intergenic locus on 7p15.2 that was genome-wide signific

62 ts were found for the putamen, where a novel intergenic locus with replicable influence on volume (rs

63 rmed on human left/right pairs identified an intergenic long noncoding RNA adjacent to the PITX2 gene

64 identification of 145 previously unannotated intergenic long noncoding RNA transcripts (lncRNA) or is

65 Recently, a handful of intergenic long noncoding RNAs (lncRNAs) have been shown

66 Distal intronic and 3' intergenic loop formations competed with repressor eleme

67 ated 300-500 kb upstream of their associated intergenic microRNAs, suggesting that distal regulatory

68 d provides accurate TSS prediction for human intergenic miRNAs at a high resolution.

69 PRO-seq experiments identified TSSs for 480 intergenic miRNAs, indicating a wide usage of alternativ

70 The challenge of linking intergenic mutations to target genes has limited molecul

71 signatures of selection on nonsynonymous or intergenic mutations.

72 ings identify Neat1 as a p53-regulated large intergenic ncRNA (lincRNA) with a key role in suppressin

73 o the recently described vlincRNA (very long intergenic ncRNA) class are mainly activated.

74 onic unprocessed transcript, as well as long intergenic non-coding (lincRNAs) and enhancer-associated

75 f a newly identified vast class of very long intergenic non-coding (vlinc) RNAs.

76 ction of microRNAs (miRNAs) are derived from intergenic non-coding loci and the identification of the

77 association between polymorphisms in a long intergenic non-coding RNA (lincRNA) gene (AC011288.2) an

78 LincRNA-p21 is a long intergenic non-coding RNA (lincRNA) involved in the p53-

79 hibit distinct messenger RNA (mRNA) and long intergenic non-coding RNA (lincRNA) profiles compared to

80 genes simultaneously, and to upregulate long intergenic non-coding RNA (lincRNA) transcripts.

81 In patients with type 2 diabetes, long intergenic non-coding RNA predicting cardiac remodeling

82 ication and characterization of a novel long intergenic non-coding RNA with MyoD-regulated and skelet

83 than 3 billion reads identified 22 334 long intergenic non-coding RNAs (lincRNAs) and 6673 pairs of

84 Long intergenic non-coding RNAs (lincRNAs) are transcribed fr

85 ematic investigation of the capacity of long intergenic non-coding RNAs (lincRNAs) as biomarkers asso

86 Long intergenic non-coding RNAs (lincRNAs) associated with a

87 341 intergenic non-coding RNAs, together with novel exons of

88 transcriptome to detect 6,701 putative long intergenic non-coding transcripts (lincRNAs) expressed i

89 deletion-based approach identified two long intergenic non-coding(linc)RNAs, lincRNA-Cox2 and lincRN

90 Expression of long intergenic non-protein coding RNA 518 (LINC00518) and pr

91 e describe the identification of 30 550 long intergenic noncoding RNA (lincRNA) loci (50 566 transcri

92 haracterize the 3D organization of 998 large intergenic noncoding RNA (lincRNA) promoters in two huma

93 o the A-bodies by interacting with ribosomal intergenic noncoding RNA (rIGSRNA).

94 e demonstrate that betalinc1 (beta-cell long intergenic noncoding RNA 1), a conserved lncRNA, is nece

95 ong noncoding RNA (lncRNA) Flicr (Foxp3 long intergenic noncoding RNA) is a negative regulator that t

96 While long intergenic noncoding RNAs (lincRNAs) and mRNAs share sim

97 Long intergenic noncoding RNAs (lincRNAs) are derived from th

98 Long intergenic noncoding RNAs (lincRNAs) are emerging as imp

99 Long intergenic noncoding RNAs (lincRNAs) are important regul

100 Long intergenic noncoding RNAs (lincRNAs) are increasingly re

101 Long intergenic noncoding RNAs (lincRNAs) are increasingly re

102 Long intergenic noncoding RNAs (lincRNAs) are long noncoding

103 tein-coding domains could help identify long intergenic noncoding RNAs (lincRNAs) associated with met

104 Long intergenic noncoding RNAs (lincRNAs) can regulate the tr

105 xtent to which alternative splicing and long intergenic noncoding RNAs (lincRNAs) contribute to the s

106 ese noncoding RNAs, a growing number of long intergenic noncoding RNAs (lincRNAs) have been described

107 Long intergenic noncoding RNAs (lincRNAs) play important role

108 protein-coding genes, and 567 putative long intergenic noncoding RNAs.

109 nally, we identify a multitude of novel long intergenic nonprotein coding RNAs (lincRNAs) specificall

110 sized that copy number alterations (CNAs) of intergenic nonprotein-coding domains could help identify

111 HPRT1 function was robust to deletion of any intergenic or deeply intronic non-coding region, indicat

112 erein as non-3UTR), as well as antisense and intergenic polyadenlation.

113 ion for the genetic association of HBS1L-MYB intergenic polymorphisms with human erythroid traits and

114 ction of antisense RNA, influences psbT/psbH intergenic processing.

115 among populations was largely attributed to intergenic recombination.

116 re we document that the arenavirus noncoding intergenic region (IGR) has a high degree of plasticity

117 The intergenic region (IGR) IRES adopts an unusual structure

118 The intergenic region (IGR) IRESs from the Dicistroviridae f

119 proach involved replacement of the noncoding intergenic region (IGR) of the L genome segment with the

120 We have recently shown that the noncoding intergenic region (IGR) present in each arenavirus genom

121 on and a point mutation within the L-segment intergenic region (IGR), and three silent changes in the

122 located in 5 untranslated region (uPSS) and intergenic region (iPSS), respectively.

123 strongest is located on chromosome 2, in an intergenic region 35- to 80-kb upstream from the thyroid

124 RH50 binds to transcripts of the 23S-4.5S intergenic region and, in its absence, levels of the cor

125 One of these, at chromosome 11p13, is an intergenic region between Ets homologous factor (EHF) an

126 ated within a predicted super-enhancer in an intergenic region between HLA-DRB1 and HLA-DQA1, localiz

127 regions go through substantial changes: the intergenic region between NP and VP35, as well as the fi

128 located upstream of oppB and one within the intergenic region between oppF and oppA.

129 entified 28 targets of PA2588, including the intergenic region between PA2588 and pqsH, which encodes

130 Tandem repeats were frequently found in the intergenic region between the prophage at the 3' end and

131 G, NID1, DHRS12, ITPK1, ACSF3, TNFRSF13C and intergenic region chr10p12.31 was replicated in a cohort

132 contains hundreds of V(H)s, separated by an intergenic region from Igh Ds, J(H)s, and constant regio

133 ), HDL-cholesterol (PHOSPHO1, SYNGAP1 and an intergenic region in chromosome 2) and triglycerides (MY

134 The dicistrovirus intergenic region internal ribosome entry site (IRES) ad

135 single-nucleotide polymorphisms (SNPs) in an intergenic region located between the oncogenes MYC and

136 d rs11048230 (P=4.77x10(-8); MAF=0.10) in an intergenic region near RASSF8 (associated with vascular

137 .71 x 10(-10), rs16891982), and revealed the intergenic region of BEND7 and PRPF18 as a novel locus a

138 The SNP rs17645023 located in the intergenic region of CACNG4 and CACNG5 was identified to

139 An intergenic region of human chromosome 2 (2p25.3) harbors

140 Linc-RAM is transcribed from an intergenic region of myogenic cells and its expression i

141 gle nucleotide polymorphism at the trnL-trnF intergenic region of the chloroplast chromosome was conf

142 ription start site was identified within the intergenic region of the miR-183 cluster, which may regu

143 t cancer risk is strongly associated with an intergenic region on 11q13.

144 gnificant associations at two novel loci: an intergenic region on 9p21.3 (rs12553324, P = 5.87 x 10 (

145 nflammatory states, maps to the 5' end of an intergenic region on Chr11p13 that is implicated as a mo

146 olymorphisms (SNPs) (r(2)>0.9) located in an intergenic region on chromosome 3q26 were associated wit

147 d loci (CAV1-CAV2, CDKN2B-AS1, SIX1-SIX6, an intergenic region on chromosome 8q22, ABCA1, GAS7, AFAP1

148 ic control region 1 (IGCR1) in the V(H)-to-D intergenic region regulates Igh V(D)J recombination in t

149 pendent reporter gene cassette located in an intergenic region remained silent, indicating that the t

150 f a 605-bp region within the RPA135-tK(CUU)P intergenic region results in a reduction in the RPA135-I

151 S_NmUC isolates was an IS1301 element in the intergenic region separating the capsule ctr-css operons

152 NA genome, with an 827 nt-long 5' UTR and an intergenic region separating two open reading frames.

153 indromic (REP) elements within the yqjH-yqjI intergenic region shows that these sequences are not req

154 a 75-bp sequence within the RPA135-tK(CUU)P intergenic region that is involved in the interaction.

155 In EAs, one chromosome 7 intergenic region was genome-wide significant (GWS): rs1

156 Six of these genes and 1 intergenic region were new discoveries showing different

157 4.8 kb miR-183 family cluster, including the intergenic region which contains highly conserved genomi

158 We show that XdhR binds the xdhABC-xdhR intergenic region with high affinity (Kd approximately 0

159 coding RNA complementary to the 4.5S-5S rRNA intergenic region, and its presence correlated with that

160 odels included SNPs in BCL11A, the HBS1L-MYB intergenic region, and the site of the HBB gene cluster,

161 n of a 198-nucleotide sequence into the HN-L intergenic region, resulting in reduced viral gene expre

162 We applied this methodology to the HBS1L-MYB intergenic region, which is associated with red-blood-ce

163 with a transposon insertion in the upstream intergenic region, while FT2c and FT2d obtained a transp

164 s), and 68 meningococci had the capsule-null intergenic region.

165 osite orientations, separated by a noncoding intergenic region.

166 on the opposite DNA strand in the psbT/psbH intergenic region.

167 dentified signals include two that reside in intergenic regions (1q31.1 and 5p13.1) and three residin

168 Nontranslated intergenic regions (IGRs) compose 10-15% of bacterial ge

169 the most abundant sRNAs transcribed from the intergenic regions (IGRs) of the bacterial genome.

170 The viral genes either are separated by intergenic regions (IRs) of variable length or overlap.

171 orders, including short (4- or 5-nucleotide) intergenic regions (IRs), a single long (144-nucleotide)

172 division of two groups were mp and the large intergenic regions (LIR).

173 s well as inside Rep and cp and in the short intergenic regions (SIR).

174 border regions between domains contain large intergenic regions and a high density of transcription f

175 ng transcriptionally silent chromatin within intergenic regions and at the border of euchromatin and

176 al activity in most non-PcG target genes and intergenic regions and is governed by opposing roaming a

177 i-cistronic operons with rationally designed intergenic regions and systematically increased upstream

178 (rRNA) processing, many coding sequences and intergenic regions appeared to be direct targets of RNas

179 er through the realization that mutations in intergenic regions are actually within unannotated small

180 ell embryos is highly promiscuous, such that intergenic regions are extensively expressed and thousan

181 The intergenic regions between PA4203 and ppgL and between P

182 The eukaryotic genome has vast intergenic regions containing transposons, pseudogenes,

183 DNAm sites located in intergenic regions had a higher mean DNAm level and were

184 that control pervasive transcription within intergenic regions have not been well established.

185 f somatic mutation across exons, introns and intergenic regions highlights the repertoire of cancer g

186 (TUCs) along the genomic sequence; (ii) the intergenic regions in front of the first gene of each TU

187 creases in promoter regions and decreases in intergenic regions in pre-iPSCs, then recovers to an int

188 Conservation of these intergenic regions in spatiotemporally separated Trichod

189 Microsatellite mapping found a bias toward intergenic regions in the nonconserved microsatellites a

190 t microsatellite mapping found a bias toward intergenic regions in the nonconserved microsatellites a

191 ong noncoding transcripts (>200 nt) from the intergenic regions of annotated protein-coding genes.

192 genomes shows many cases of association with intergenic regions of genes with altered expression due

193 rs and enhancers, ultraconserved regions and intergenic regions of protein-coding genes.

194 and un-annotated exon boundaries, including intergenic regions of the genome, with high statistical

195 ferentially distributed over gene bodies and intergenic regions of the genome.

196 several CpG sites primarily localized in the intergenic regions of the genome.

197 we developed a custom script that can detect intergenic regions of the S. pyogenes genome.

198 r 44 traits studied are novel and located in intergenic regions or introns of genes.

199 regulated loci correspond to transposons and intergenic regions producing 24-nucleotide siRNAs that g

200 RNAs (piRNAs), yet the functions of the vast intergenic regions remain largely unknown.

201 BCG1, CPT1A, MYLIP, TXNIP and SLC7A11) and 2 intergenic regions showed differential methylation in as

202 ed by RNA polymerase II and map to low-copy, intergenic regions similar to PIWI-interacting RNAs (piR

203 cted, nucleotide diversity is much higher in intergenic regions than within gene bodies (regions span

204 evising several methods to select subsets of intergenic regions that can concentrate these rare RNA c

205 To identify a comprehensive set of genes and intergenic regions that impacts fitness in S. elongatus,

206 icient resolution in the larger intronic and intergenic regions to identify copy number changes.

207 han 900 validated bacterial sRNAs and 23,000 intergenic regions were analyzed.

208 DMRs located within intergenic regions were heavily enriched for AP-1 transc

209 Stringtie was then performed to identify the intergenic regions whose expression was influenced by th

210 These loci are mostly in intergenic regions with dense DNA methylation.

211 Intergenic regions within the unique long 52 gene (UL52;

212 ores, enriched within gene bodies but not in intergenic regions, and preferentially harbored binding

213 bserve that the genome is more accessible in intergenic regions, and that increased accessibility is

214 introns), while being depleted in coding and intergenic regions, and these findings may have biologic

215 ber of genes, together with transcripts from intergenic regions, are up-regulated.

216 t may be transcribed: coding, noncoding, and intergenic regions, as well as repetitive elements, telo

217 ion in CpG island (CGI) and demethylation in intergenic regions, defined as 'backbone', largely vary

218 Approximately 1500 intergenic regions, displaying low DNA methylation, high

219 d are more likely to occur in the genic than intergenic regions, especially common in the 5'- and 3'-

220 ociated haplotype blocks are in intronic and intergenic regions, hindering their functional evaluatio

221 5' and 3' untranslated regions as well as in intergenic regions, identification and validation of tru

222 WAS) appear to be located within intronic or intergenic regions, which makes it difficult to interpre

223 majority of detected heteroplasmies occur in intergenic regions.

224 -enhancers demonstrated extensive binding at intergenic regions.

225 tion start sites, within gene bodies, and in intergenic regions.

226 moters in gene bodies and non-coding RNAs in intergenic regions.

227 matin accessibility at a large subset of the intergenic regions.

228 ally targets transposable elements (TEs) and intergenic regions.

229 trand switch regions, telomeric regions, and intergenic regions.

230 ted leader sequences, antisense strands, and intergenic regions.

231 ination bias toward both high GC content and intergenic regions.

232 ncoding RNAs, regulatory elements, and other intergenic regions.

233 gnition of DNA photoproducts, prevalently in intergenic regions.

234 Five states map mainly to genes and five to intergenic regions.

235 oter-proximal regions to the gene bodies and intergenic regions.

236 s selected more features from non-CpG island intergenic regions.

237 D hotspots occur almost equally in genic and intergenic regions.

238 pped reads were also found from intronic and intergenic regions.

239 1, DHRS12, ITPK1, ACSF3 and TNFRSF13C, and 2 intergenic regions.

240 ier microsatellite loci located in conserved intergenic regions.

241 hylation are localized to CpG islands within intergenic regions.

242 ne expression by altering the copy number of intergenic regulatory regions.

243 atory regions as well as with Pax5-activated intergenic repeat elements and 5' distal VH genes were c

244 during early S phase followed by most of the intergenic repetitive regions replicating during middle

245 long noncoding RNA, Hox transcript antisense intergenic RNA (HOTAIR).

246 s a result of ribosome-assisted unfolding of intergenic RNA structures.

247 NAs, LL18/NANCI (Nkx2.1-associated noncoding intergenic RNA) and LL34, play distinct roles in endoder

248 study, we report that HOTAIR (HOX antisense intergenic RNA) is upregulated in tamoxifen-resistant br

249 lncRNA) HOTAIR (for HOX Transcript Antisense Intergenic RNA) mediates a physical interaction between

250 ithin the NANCI (Nkx2.1-associated noncoding intergenic RNA)-Nkx2.1 gene duplex that is essential for

251 s of non-coding RNA including microRNA, long intergenic RNA, small nucleolar RNA, natural antisense t

252 unique expression of coding, noncoding, and intergenic RNAs in the mature mouse brain with RNA-Seq a

253 of the ribosomal DNA (rDNA) repeats and the intergenic sequence between the locus encoding the secon

254 enome sizes were mainly due to variations in intergenic sequence length.

255 uit fly Drosophila melanogaster relies on an intergenic sequence termed the IRER (irradiation-respons

256 tions in cancer have identified mutations in intergenic sequences encoding regulatory elements-and in

257 duction near genes compared with the rest of intergenic sequences is greater in a species with larger

258 utative mammary-specific enhancer within the intergenic sequences separating the two Stat5 genes.

259 gapless coverage over gene space as well as intergenic sequences such as centromeres, telomeres, tra

260 ntiation, the preferred targets are intronic/intergenic sequences with enhancer-like activity.

261 fragmented, lacking skewed GC and repetitive intergenic sequences, which are gaining importance due t

262 An intergenic single-nucleotide polymorphism (rs4445257) on

263 An intergenic single-nucleotide polymorphism on chromosome

264 here dI is the number of intergenic SNPs per intergenic site.

265 th of purifying selection operating over all intergenic sites is consistently intermediate between th

266 observed in addicted rats occurred mostly at intergenic sites located on long and short interspersed

267 The results showed that one intergenic SNP (rs11901793), which is 20 kb upstream of

268 e an intronic SNP in FOXP1 at locus 3p13, an intergenic SNP at 3q28 near TP63, and an intergenic SNP

269 an intergenic SNP at 3q28 near TP63, and an intergenic SNP at 9p22 near BNC2.

270 etween LSLs and the maternal genotype for an intergenic SNP on chromosome 10 (rs11008222, combined P

271 n between LSLs and the case genotype for one intergenic SNP on chromosome 16 achieved genome-wide sig

272 d the dI/dS ratio, where dI is the number of intergenic SNPs per intergenic site.

273 Despite 10-fold variation in intergenic space among species, the majority of open chr

274 that contained a transposon inserted in the intergenic space between sufC and sufD (sufD*), resultin

275 n to amplify a variable region of the 23S-5S intergenic spacer (IGS) ofRickettsiaspp.

276 Despite preserved intergenic spacer (IGS) structure, they showed altered c

277 nged in head-to-tail fashion separated by an intergenic spacer (IGS).

278 ng peak height thresholds for automated rRNA intergenic spacer analysis (ARISA) profiles.

279 iled for bacterial diversity using ribosomal intergenic spacer analysis (RISA) PCR.

280 One large 101 bp intergenic spacer between trnY and cox1 was in S. varius

281 es cerevisiae genome that occurs between the intergenic spacer of the ribosomal DNA (rDNA) repeats an

282 microsatellites loci (nSSRs) and three cpDNA intergenic spacer regions.

283 These large intergenic spacers may have developed during intervals o

284 noncoding RNAs from the ribosomal DNA (rDNA) intergenic spacers, consistent with its previously repor

285 and notable improvements in the assembly of intergenic spaces and centromeres.

286 P2 and other latency-associated transcripts, intergenic splicing at the BZLF2 locus, and antisense tr

287 and into downstream genes, leading to novel intergenic splicing between exons of neighbouring cellul

288 splicing sites, thus are likely products of 'intergenic splicing'.

289 topographical relationships revealed that an intergenic state, characterized by H3K27me3 and slightly

290 sed the potential functional implications of intergenic SVs.

291 ammatory conditions via the production of an intergenic transcript linking neuronal and immune Fpr ge

292 Within these domains, intergenic transcriptional enhancers evade heterochromat

293 a novel human locus, H11, located in a safe, intergenic, transcriptionally active region of chromosom

294 anscriptional output at both known mRNAs and intergenic transcripts.

295 n OPCML (P=9.89 x 10(-6)), and rs7700147, an intergenic variant (P=2.93 x 10(-5)).

296 authors discovered 2 novel AF variants, the intergenic variant rs72700114, between the genes LINC011

297 We found that several HBS1L-MYB intergenic variants reduce transcription factor binding,

298 summary, we identified and characterized an intergenic VNTR polymorphism in S. pyogenes that affects

299 Here, we report an intergenic VNTR polymorphism that confers an altered lev

300 and silencing were used to identify a novel intergenic Y-linked lncRNA, named lnc-KDM5D-4, and inves